A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028195



Internal ID19117413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61255381..62369822hg19UCSC Ensembl
Innerchr7:61259323..62007257hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg191114442
hg18747935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6391n100
Supporting Variantsnssv3661563, nssv3661564
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)nsv1028195
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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