A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019278



Internal ID19108496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155263540..155284018hg38UCSC Ensembl
Innerchr7:155055250..155075728hg19UCSC Ensembl
Innerchr7:154686183..154706661hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3820479
hg1920479
hg1820479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6766n100
Supporting Variantsnssv3674693, nssv3674694
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)nsv1019278
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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