A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020784



Internal ID18763318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83948086..84057792hg38UCSC Ensembl
Innerchr7:83577402..83687108hg19UCSC Ensembl
Innerchr7:83415338..83525044hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38109707
hg19109707
hg18109707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755421
Samples
Known GenesSEMA3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020784
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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