A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700055



Internal ID15436707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110492552..110496218hg38UCSC Ensembl
Innerchr1:111035174..111038840hg19UCSC Ensembl
Innerchr1:110836697..110840363hg18UCSC Ensembl
Innerchr1:110747216..110750882hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383667
hg193667
hg183667
hg173667
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700055
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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