A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492805



Internal ID22550733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21104469..21108685hg38UCSC Ensembl
chr4:21106092..21110308hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg384217
hg194217
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838637
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492805
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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