A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140692



Internal ID339885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52943794..52945218hg38UCSC Ensembl
chr6:52808592..52810016hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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