A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705629



Internal ID15442281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161159500..161163351hg38UCSC Ensembl
Innerchr6:161580532..161584383hg19UCSC Ensembl
Innerchr6:161500522..161504373hg18UCSC Ensembl
Innerchr6:161550943..161554794hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383852
hg193852
hg183852
hg173852
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528938
Supporting Variants
Samples
Known GenesAGPAT4, AGPAT4-IT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705629
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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