A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701490



Internal ID15091456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:69896150..69901404hg38UCSC Ensembl
Innerchr1:70361833..70367087hg19UCSC Ensembl
Innerchr1:70134421..70139675hg18UCSC Ensembl
Innerchr1:70073854..70079108hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385255
hg195255
hg185255
hg175255
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525370
Supporting Variants
Samples
Known GenesLRRC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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