A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658959



Internal ID15048925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110486946..110494095hg38UCSC Ensembl
Innerchr1:111029568..111036717hg19UCSC Ensembl
Innerchr1:110831091..110838240hg18UCSC Ensembl
Innerchr1:110741610..110748759hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387150
hg197150
hg187150
hg177150
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519826
Supporting Variants
Samples
Known GenesCYMP, LOC440602
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658959
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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