A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034234



Internal ID19123456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61255381..62393418hg19UCSC Ensembl
Innerchr7:61259323..62030853hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg191138038
hg18771531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6391n100
Supporting Variantsnssv3661565
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)nsv1034234
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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