A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492465



Internal ID22550392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44651692..44652991hg38UCSC Ensembl
chr3:44693184..44694483hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835983
Supporting Variants
Samples
Known GenesZNF35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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