A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545679



Internal ID15986402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16908642..16932783hg38UCSC Ensembl
Innerchr1:17235137..17259278hg19UCSC Ensembl
Innerchr1:17107724..17131865hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3824142
hg1924142
hg1824142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv168n54
Supporting Variantsnssv710907
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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