A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562770



Internal ID16350179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95277634..95320242hg38UCSC Ensembl
Innerchr13:95929888..95972496hg19UCSC Ensembl
Innerchr13:94727889..94770497hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3842609
hg1942609
hg1842609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148679
SamplesHGDP00720
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562770
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer