A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017184



Internal ID19106401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109600044..109709954hg38UCSC Ensembl
Innerchr7:109240101..109350011hg19UCSC Ensembl
Innerchr7:109027337..109137247hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38109911
hg19109911
hg18109911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656233
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)nsv1017184
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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