A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140247



Internal ID339440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:151587618..151594600hg38UCSC Ensembl
chr2:152444132..152451114hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg386983
hg196983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16925497
Samples
Known GenesNEB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140247
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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