A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492804



Internal ID22550732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21104468..21107873hg38UCSC Ensembl
chr4:21106091..21109496hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383406
hg193406
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839179
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492804
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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