A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667062



Internal ID15057028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34470157hg38UCSC Ensembl
Innerchr15:34718594..34762358hg19UCSC Ensembl
Innerchr15:32505886..32549650hg18UCSC Ensembl
Innerchr15:32505886..32549650hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3843765
hg1943765
hg1843765
hg1743765
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667062
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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