A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637615



Internal ID6677718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356693..1364925hg38UCSC Ensembl
chr16:1406694..1414926hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388233
hg198233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv473e214
Supporting Variantsessv15359755, essv15359754, essv15359753, essv15359756, essv15359752
SamplesHG03517, HG02922, HG00629, HG00266, HG03511
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637615
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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