A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497669



Internal ID22555603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170362578..170434914hg38UCSC Ensembl
chr5:169789582..169861918hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3872337
hg1972337
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842118
Supporting Variants
Samples
Known GenesKCNIP1, KCNMB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497669
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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