A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664886



Internal ID15054852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113096943..113104996hg38UCSC Ensembl
Innerchr9:115859223..115867276hg19UCSC Ensembl
Innerchr9:114899044..114907097hg18UCSC Ensembl
Innerchr9:112938777..112946830hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg388054
hg198054
hg188054
hg178054
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515822
Supporting Variants
Samples
Known GenesFAM225B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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