A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523467



Internal ID15104074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:151999947..152001288hg38UCSC Ensembl
Innerchr7:151697032..151698373hg19UCSC Ensembl
Innerchr7:151327965..151329306hg18UCSC Ensembl
Innerchr7:151134680..151136021hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381342
hg191342
hg181342
hg171342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699226
Samples
Known GenesGALNTL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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