A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525499



Internal ID18823780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95287620..95364191hg38UCSC Ensembl
Innerchr13:95939874..96016445hg19UCSC Ensembl
Innerchr13:94737875..94814446hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3876572
hg1976572
hg1876572
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044131
Supporting Variants
Samples
Known GenesABCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525499
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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