A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662214



Internal ID18960495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133722836..133978125hg38UCSC Ensembl
Innerchr7:133407589..133662878hg19UCSC Ensembl
Innerchr7:133058129..133313418hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38255290
hg19255290
hg18255290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028914
Supporting Variants
Samples
Known GenesEXOC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662214
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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