A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008178



Internal ID19097397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76317328..76359206hg38UCSC Ensembl
Innerchr2:76544454..76586332hg19UCSC Ensembl
Innerchr2:76397962..76439840hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3841879
hg1941879
hg1841879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3873n100
Supporting Variantsnssv3582008
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)nsv1008178
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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