A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587628



Internal ID6627929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155619701..155695480hg38UCSC Ensembl
chr1:155589492..155665271hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3875780
hg1975780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10152267
SamplesNA20761
Known GenesDAP3, YY1AP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587628
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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