A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705978



Internal ID15442630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89452888..89454756hg38UCSC Ensembl
Innerchr9:92067803..92069671hg19UCSC Ensembl
Innerchr9:91257623..91259491hg18UCSC Ensembl
Innerchr9:89297357..89299225hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381869
hg191869
hg181869
hg171869
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517495
Supporting Variants
Samples
Known GenesSEMA4D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705978
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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