A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997843



Internal ID18810693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61970416..61981630hg38UCSC Ensembl
Innerchr1:62436088..62447302hg19UCSC Ensembl
Innerchr1:62208676..62219890hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3811215
hg1911215
hg1811215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169n100
Supporting Variantsnssv3464503
Samples
Known GenesINADL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997843
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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