A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603249



Internal ID21795296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61387891..61389115hg38UCSC Ensembl
chr14:61854609..61855833hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040223
Supporting Variants
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603249
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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