A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008207



Internal ID18750738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8751759..8811395hg38UCSC Ensembl
Innerchr2:8891889..8951525hg19UCSC Ensembl
Innerchr2:8809340..8868976hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3859637
hg1959637
hg1859637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576950
Samples
Known GenesKIDINS220
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008207
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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