A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025306



Internal ID19114524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756249..97775599hg38UCSC Ensembl
Innerchr7:97385561..97404911hg19UCSC Ensembl
Innerchr7:97223497..97242847hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3819351
hg1919351
hg1819351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6535n100
Supporting Variantsnssv3655273
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)nsv1025306
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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