A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364598



Internal ID22590267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119380601..119380736hg38UCSC Ensembl
chr1:119923224..119923359hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877399
Supporting Variants
Samples
Known GenesHAO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364598
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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