A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139802



Internal ID338991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85300376..85357603hg38UCSC Ensembl
chr3:85349526..85406753hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3857228
hg1957228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935990
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139802
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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