A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028743



Internal ID19117961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61272656..62978903hg38UCSC Ensembl
Innerchr7:61255381..62439281hg19UCSC Ensembl
Innerchr7:61259323..62076716hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381706248
hg191183901
hg18817394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6391n100
Supporting Variantsnssv3661566
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)nsv1028743
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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