A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030363



Internal ID18772894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3501414..3538033hg38UCSC Ensembl
Innerchr7:3541046..3577665hg19UCSC Ensembl
Innerchr7:3507572..3544191hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3836620
hg1936620
hg1836620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654988
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030363
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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