A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719765



Internal ID15667035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103579934..103630590hg38UCSC Ensembl
Innerchr1:104122556..104173212hg19UCSC Ensembl
Innerchr1:103924079..103974735hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3850657
hg1950657
hg1850657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546981
Supporting Variants
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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