A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695825



Internal ID15085791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77242359..77283166hg38UCSC Ensembl
Innerchr18:74954315..74995122hg19UCSC Ensembl
Innerchr18:73083303..73124110hg18UCSC Ensembl
Innerchr18:73083303..73124110hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3840808
hg1940808
hg1840808
hg1740808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518395
Supporting Variants
Samples
Known GenesGALR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695825
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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