A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024118



Internal ID19113335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:964887..1022730hg38UCSC Ensembl
Innerchr7:1004523..1062366hg19UCSC Ensembl
Innerchr7:971049..1028892hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3857844
hg1957844
hg1857844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752786
Samples
Known GenesC7orf50, COX19, CYP2W1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024118
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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