A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725963



Internal ID19024244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36109464..36204248hg38UCSC Ensembl
Innerchr2:36336607..36431391hg19UCSC Ensembl
Innerchr2:36190111..36284895hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3894785
hg1994785
hg1894785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013801
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)nssv3725963
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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