A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009926



Internal ID18752457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61973547..61989112hg38UCSC Ensembl
Innerchr1:62439219..62454784hg19UCSC Ensembl
Innerchr1:62211807..62227372hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815566
hg1915566
hg1815566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv170n100
Supporting Variantsnssv3468885
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)nsv1009926
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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