A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv716175



Internal ID16010131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72089806..72217543hg38UCSC Ensembl
Innerchr1:72555489..72683226hg19UCSC Ensembl
Innerchr1:72328077..72455814hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38127738
hg19127738
hg18127738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546481
Supporting Variants
Samples
Known GenesNEGR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv716175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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