A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020837



Internal ID18763371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100715499..100911015hg38UCSC Ensembl
Innerchr7:100313122..100508635hg19UCSC Ensembl
Innerchr7:100151058..100346571hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38195517
hg19195514
hg18195514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655297
Samples
Known GenesACHE, EPHB4, EPO, MIR6875, SLC12A9, SRRT, TRIP6, UFSP1, ZAN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020837
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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