A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028190



Internal ID19117408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110512818..110557355hg38UCSC Ensembl
Innerchr7:110152875..110197412hg19UCSC Ensembl
Innerchr7:109940111..109984648hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3844538
hg1944538
hg1844538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6563n100
Supporting Variantsnssv3751481
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)nsv1028190
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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