A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139334



Internal ID338519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202102797..202103381hg38UCSC Ensembl
chr1:202071925..202072509hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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