A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv729114



Internal ID16023070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:177466267..177660588hg38UCSC Ensembl
Innerchr1:177435403..177629723hg19UCSC Ensembl
Innerchr1:175702026..175896346hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38194322
hg19194321
hg18194321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548251
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)nssv729114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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