A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019113



Internal ID18761647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160706552..160776526hg38UCSC Ensembl
Innerchr6:161127584..161197558hg19UCSC Ensembl
Innerchr6:161047574..161117548hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3869975
hg1969975
hg1869975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654507
Samples
Known GenesPLG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019113
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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