A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678781



Internal ID15068747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5306824..5324922hg38UCSC Ensembl
Innerchr9:5306824..5324922hg19UCSC Ensembl
Innerchr9:5296824..5314922hg18UCSC Ensembl
Innerchr9:5296824..5314922hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3818099
hg1918099
hg1818099
hg1718099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678781
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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