A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695736



Internal ID15432388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74943391..74950701hg38UCSC Ensembl
Innerchr9:77558307..77565617hg19UCSC Ensembl
Innerchr9:76748127..76755437hg18UCSC Ensembl
Innerchr9:74787861..74795171hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387311
hg197311
hg187311
hg177311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518305
Supporting Variants
Samples
Known GenesC9orf40
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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