A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547237



Internal ID16334646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105182577..105243024hg38UCSC Ensembl
Innerchr1:105725199..105785646hg19UCSC Ensembl
Innerchr1:105526722..105587169hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3860448
hg1960448
hg1860448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173086
SamplesNINDS_166
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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