A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv729321



Internal ID15676591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:179361849..179365666hg38UCSC Ensembl
Innerchr1:179330984..179334801hg19UCSC Ensembl
Innerchr1:177597607..177601424hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg383818
hg193818
hg183818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548296
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv729321
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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