A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv716177



Internal ID16010133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72116283..72194197hg38UCSC Ensembl
Innerchr1:72581966..72659880hg19UCSC Ensembl
Innerchr1:72354554..72432468hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3877915
hg1977915
hg1877915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546483
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)nssv716177
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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