A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603286



Internal ID21795333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88310158..88310247hg38UCSC Ensembl
chr14:88776502..88776591hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023695
Supporting Variants
Samples
Known GenesKCNK10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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