A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667307



Internal ID15057273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122481269..122483301hg38UCSC Ensembl
Innerchr10:124240785..124242817hg19UCSC Ensembl
Innerchr10:124230775..124232807hg18UCSC Ensembl
Innerchr10:124230775..124232807hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
hg172033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516138
Supporting Variants
Samples
Known GenesHTRA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667307
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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