A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546937



Internal ID16334346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102973239..103082941hg38UCSC Ensembl
Innerchr1:103438795..103548497hg19UCSC Ensembl
Innerchr1:103211383..103321085hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38109703
hg19109703
hg18109703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv389n54
Supporting Variantsnssv1173077
SamplesNINDS_160
Known GenesCOL11A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546937
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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