A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334222



Internal ID20867405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117100223..117440236hg38UCSC Ensembl
chr1:117642845..117982858hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38340014
hg19340014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv318n223
Supporting Variantsnssv18199756
Samples
Known GenesMAN1A2, TRIM45, TTF2, VTCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334222
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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