A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030933



Internal ID18773465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38246914..38286323hg38UCSC Ensembl
Innerchr7:38286515..38325924hg19UCSC Ensembl
Innerchr7:38253040..38292449hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3839410
hg1939410
hg1839410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6322n100
Supporting Variantsnssv3643428
Samples
Known GenesTARP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030933
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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