A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142235



Internal ID341435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14979969..15057007hg38UCSC Ensembl
chr10:15021968..15099006hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3877039
hg1977039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032038
Samples
Known GenesOLAH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142235
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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