A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023571



Internal ID19112788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159227414..159313443hg38UCSC Ensembl
Innerchr7:159020104..159106132hg19UCSC Ensembl
Innerchr7:158712865..158798893hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3886030
hg1986029
hg1886029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6779n100
Supporting Variantsnssv3674824
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)nsv1023571
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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