A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523285



Internal ID15103892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:123956..200682hg38UCSC Ensembl
Innerchr7:123956..200682hg19UCSC Ensembl
Innerchr7:219039..295765hg18UCSC Ensembl
Innerchr7:219039..295765hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3876727
hg1976727
hg1876727
hg1776727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699024
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523285
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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