A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704083



Internal ID15440735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36137349..36140118hg38UCSC Ensembl
Innerchr9:36137346..36140115hg19UCSC Ensembl
Innerchr9:36127346..36130115hg18UCSC Ensembl
Innerchr9:36127346..36130115hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382770
hg192770
hg182770
hg172770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527617
Supporting Variants
Samples
Known GenesGLIPR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704083
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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