A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637614



Internal ID7024405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356674..1364974hg38UCSC Ensembl
Innerchr16:1356674..1364974hg38UCSC Ensembl
Outerchr16:1356617..1365011hg38UCSC Ensembl
chr16:1406675..1414975hg19UCSC Ensembl
Innerchr16:1406675..1414975hg19UCSC Ensembl
Outerchr16:1406618..1415012hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388301
hg198301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv473e214
Supporting Variantsessv15359749, essv15359750, essv15359751
SamplesHG03517, HG02922, HG03511
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637614
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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