A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704736



Internal ID15094702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34450638hg38UCSC Ensembl
Innerchr15:34718594..34742839hg19UCSC Ensembl
Innerchr15:32505886..32530131hg18UCSC Ensembl
Innerchr15:32505886..32530131hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3824246
hg1924246
hg1824246
hg1724246
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv704736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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