A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726664



Internal ID19024945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4155585..4176417hg38UCSC Ensembl
Innerchr2:4203175..4224007hg19UCSC Ensembl
Innerchr2:4181050..4201882hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3820833
hg1920833
hg1820833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998778
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)nssv3726664
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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