A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701416



Internal ID15438068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136031934..136038210hg38UCSC Ensembl
Innerchr9:138923780..138930056hg19UCSC Ensembl
Innerchr9:138063601..138069877hg18UCSC Ensembl
Innerchr9:136149725..136156001hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386277
hg196277
hg186277
hg176277
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525309
Supporting Variants
Samples
Known GenesNACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701416
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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