A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493628



Internal ID22551557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17591313..17593862hg38UCSC Ensembl
chr4:17592936..17595485hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838449
Supporting Variants
Samples
Known GenesLAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493628
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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