A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497644



Internal ID22555578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169644988..169650292hg38UCSC Ensembl
chr5:169071992..169077296hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385305
hg195305
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842117
Supporting Variants
Samples
Known GenesDOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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