A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903808



Internal ID3356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58102364..58115871hg38UCSC Ensembl
chr1:58568036..58581543hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3813508
hg1913508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432284
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903808
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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