A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031478



Internal ID19120700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142314620..142345098hg38UCSC Ensembl
Innerchr7:142014445..142044929hg19UCSC Ensembl
Innerchr7:141660939..141691401hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3830479
hg1930485
hg1830463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3667857
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031478
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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