A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586870



Internal ID18538465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:231478058..231638882hg38UCSC Ensembl
Innerchr2:232342769..232503593hg19UCSC Ensembl
Innerchr2:232051013..232211837hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38160825
hg19160825
hg18160825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999161
Supporting Variants
Samples
Known GenesC2orf57, LINC00471, NMUR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586870
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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