A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409652



Internal ID22467522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58958769..58991660hg38UCSC Ensembl
chr3:58944495..58977386hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3832892
hg1932892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900409
Supporting Variants
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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