A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026246



Internal ID18768778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62526783..63523932hg38UCSC Ensembl
Innerchr7:61987161..62984310hg19UCSC Ensembl
Innerchr7:61624596..62621745hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38997150
hg19997150
hg18997150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6397n100
Supporting Variantsnssv3753013
Samples
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026246
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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