A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702599



Internal ID15439251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14347812..14362391hg38UCSC Ensembl
Innerchr9:14347811..14362390hg19UCSC Ensembl
Innerchr9:14337811..14352390hg18UCSC Ensembl
Innerchr9:14337811..14352390hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3814580
hg1914580
hg1814580
hg1714580
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526315
Supporting Variants
Samples
Known GenesNFIB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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