A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029931



Internal ID18772462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38271110..38312626hg38UCSC Ensembl
Innerchr7:38310711..38352227hg19UCSC Ensembl
Innerchr7:38277236..38318752hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3841517
hg1941517
hg1841517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6329n100
Supporting Variantsnssv3643461
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)nsv1029931
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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