A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695015



Internal ID15084981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227885108..227900570hg38UCSC Ensembl
Innerchr1:228072809..228088271hg19UCSC Ensembl
Innerchr1:226139432..226154894hg18UCSC Ensembl
Innerchr1:224379544..224395006hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3815463
hg1915463
hg1815463
hg1715463
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516409
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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