A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023293



Internal ID19112510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63158963..63649517hg38UCSC Ensembl
Innerchr7:62619341..63109895hg19UCSC Ensembl
Innerchr7:62256776..62747330hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38490555
hg19490555
hg18490555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6432n100
Supporting Variantsnssv3661962
Samples
Known GenesLOC100287704, LOC100287834, MIR4283-1, MIR4283-2, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023293
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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