A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739490



Internal ID19037771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58222067..58482551hg38UCSC Ensembl
Innerchr4:59088233..59348717hg19UCSC Ensembl
Innerchr4:58782990..59043474hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38260485
hg19260485
hg18260485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998859
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)nssv3739490
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