A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585606



Internal ID18883887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208940937..209177848hg38UCSC Ensembl
Innerchr2:209805661..210042572hg19UCSC Ensembl
Innerchr2:209513906..209750817hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38236912
hg19236912
hg18236912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009924
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)nssv3585606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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