A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689053



Internal ID15079019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5274464..5345673hg38UCSC Ensembl
Innerchr9:5274464..5345673hg19UCSC Ensembl
Innerchr9:5264464..5335673hg18UCSC Ensembl
Innerchr9:5264464..5335673hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3871210
hg1971210
hg1871210
hg1771210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516752
Supporting Variants
Samples
Known GenesRLN1, RLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689053
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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