A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140132



Internal ID339324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134503133..134504012hg38UCSC Ensembl
chr2:135260704..135261583hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924220
Samples
Known GenesTMEM163
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140132
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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