A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998638



Internal ID19158174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4664592..4684131hg38UCSC Ensembl
Innerchr2:4712182..4731721hg19UCSC Ensembl
Innerchr2:4690057..4709596hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3819540
hg1919540
hg1819540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3709n100
Supporting Variantsnssv3576923
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)nsv998638
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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