A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020332



Internal ID18762867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142853182..142867988hg38UCSC Ensembl
Innerchr7:142550944..142565743hg19UCSC Ensembl
Innerchr7:142261066..142275865hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814807
hg1914800
hg1814800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3669487
Samples
Known GenesEPHB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020332
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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