A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3761422



Internal ID19059703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61656850hg38UCSC Ensembl
Innerchr9:44727847..44864688hg19UCSC Ensembl
Innerchr9:44667843..44804684hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38136842
hg19136842
hg18136842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034915
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3761422
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