A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016931



Internal ID19106148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38279738..38358446hg38UCSC Ensembl
Innerchr7:38319339..38398047hg19UCSC Ensembl
Innerchr7:38285864..38364572hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3878709
hg1978709
hg1878709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6331n100
Supporting Variantsnssv3643470
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)nsv1016931
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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