A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637545



Internal ID7024337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:153017..163827hg38UCSC Ensembl
chr16:203016..213826hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810811
hg1910811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv472e214
Supporting Variantsessv15354720, essv15354738, essv15354730, essv15354729, essv15354718, essv15354717, essv15354750, essv15354742, essv15354740, essv15354714, essv15354744, essv15354733, essv15354724, essv15354735, essv15354747, essv15354726, essv15354749, essv15354748, essv15354716, essv15354719, essv15354736, essv15354723, essv15354725, essv15354737, essv15354721, essv15354734, essv15354727, essv15354728, essv15354739, essv15354741, essv15354732, essv15354731, essv15354715, essv15354746, essv15354722, essv15354743, essv15354745
SamplesHG02481, HG02600, HG03018, HG03126, NA18959, NA12813, HG03572, HG03436, HG03168, HG02952, NA18498, HG03520, HG02642, HG02477, HG02164, HG03048, HG02442, NA19175, NA19184, HG02508, HG02497, NA18630, HG03021, NA18912, NA19017, HG02330, HG03833, HG03028, NA19321, HG01272, NA19786, HG03108, NA19475, NA19143, HG02938, HG01431, HG03985
Known GenesHBZ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637545
Frequency
Sample Size2504
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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