A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901984



Internal ID2121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34711690..34714125hg38UCSC Ensembl
chr1:35177291..35179726hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901984
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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