A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701734



Internal ID15438386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135992854..136021558hg38UCSC Ensembl
Innerchr9:138884700..138913404hg19UCSC Ensembl
Innerchr9:138024521..138053225hg18UCSC Ensembl
Innerchr9:136110645..136139349hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3828705
hg1928705
hg1828705
hg1728705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525592
Supporting Variants
Samples
Known GenesNACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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