A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521307



Internal ID15101914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:69817192..69822964hg38UCSC Ensembl
Innerchr1:70282875..70288647hg19UCSC Ensembl
Innerchr1:70055463..70061235hg18UCSC Ensembl
Innerchr1:69994896..70000668hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385773
hg195773
hg185773
hg175773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697913
Samples
Known GenesLRRC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521307
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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