A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024619



Internal ID19113836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109765814..109813841hg38UCSC Ensembl
Innerchr7:109405871..109453898hg19UCSC Ensembl
Innerchr7:109193107..109241134hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3848028
hg1948028
hg1848028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6550n100
Supporting Variantsnssv3656236
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)nsv1024619
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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