A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360393



Internal ID22586062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119620899..119620970hg38UCSC Ensembl
chr1:120163522..120163593hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872597
Supporting Variants
Samples
Known GenesZNF697
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360393
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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