A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571308



Internal ID18869589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4155585..4175565hg38UCSC Ensembl
Innerchr2:4203175..4223155hg19UCSC Ensembl
Innerchr2:4181050..4201030hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3819981
hg1919981
hg1819981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003168
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)nssv3571308
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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