A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632342



Internal ID7019151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61625198..61631649hg38UCSC Ensembl
chr13:62199331..62205782hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg386452
hg196452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv339e214
Supporting Variantsessv14766333, essv14766330, essv14766331, essv14766334, essv14766332
SamplesHG00766, HG02215, HG01668, HG01162, HG03631
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632342
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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