A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600903



Internal ID21792950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52918180..52918180hg38UCSC Ensembl
chr12:53311964..53311964hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094464
Supporting Variants
Samples
Known GenesKRT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600903
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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