A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730371



Internal ID19028652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:242035382..242147293hg38UCSC Ensembl
Innerchr2:242977533..243089444hg19UCSC Ensembl
Innerchr2:242626206..242738117hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38111912
hg19111912
hg18111912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008118
Supporting Variants
Samples
Known GenesLOC728323
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3730371
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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