A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890869



Internal ID168085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155537035..155552402hg38UCSC Ensembl
chr1:155506826..155522193hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3815368
hg1915368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425979
Supporting Variants
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890869
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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