A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019824



Internal ID19109042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124177113..124286800hg38UCSC Ensembl
Innerchr7:123817167..123926854hg19UCSC Ensembl
Innerchr7:123604403..123714090hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38109688
hg19109688
hg18109688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662138
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)nsv1019824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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