A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042622



Internal ID19131841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95287620..95386474hg38UCSC Ensembl
Innerchr13:95939874..96038728hg19UCSC Ensembl
Innerchr13:94737875..94836729hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3898855
hg1998855
hg1898855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1731n100
Supporting Variantsnssv3525504, nssv3525503, nssv3713282
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)nsv1042622
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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