A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019694



Internal ID19108912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38277957..38347830hg38UCSC Ensembl
Innerchr7:38317558..38387431hg19UCSC Ensembl
Innerchr7:38284083..38353956hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3869874
hg1969874
hg1869874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6331n100
Supporting Variantsnssv3643467
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019694
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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