A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358296



Internal ID22583965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173622717..173730779hg38UCSC Ensembl
chr1:173591856..173699918hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38108063
hg19108063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884019
Supporting Variants
Samples
Known GenesANKRD45, KLHL20, LOC730159
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358296
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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