A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017302



Internal ID19106519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97766136..97793614hg38UCSC Ensembl
Innerchr7:97395448..97422926hg19UCSC Ensembl
Innerchr7:97233384..97260862hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3827479
hg1927479
hg1827479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6536n100
Supporting Variantsnssv3655293, nssv3655292
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)nsv1017302
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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