A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702577



Internal ID15092543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92945910..93268110hg38UCSC Ensembl
Innerchr9:95708192..96030392hg19UCSC Ensembl
Innerchr9:94748013..95070213hg18UCSC Ensembl
Innerchr9:92787747..93109947hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38322201
hg19322201
hg18322201
hg17322201
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526296
Supporting Variants
Samples
Known GenesC9orf89, FGD3, NINJ1, SUSD3, WNK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702577
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer