A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011860



Internal ID19101078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215706919..215739740hg38UCSC Ensembl
Innerchr2:216571642..216604463hg19UCSC Ensembl
Innerchr2:216279887..216312708hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3832822
hg1932822
hg1832822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585696
Samples
Known GenesLINC00607
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011860
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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