A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283736



Internal ID20492954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52420908..52427788hg38UCSC Ensembl
chr12:52814692..52821572hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg386881
hg196881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739201
Supporting Variants
Samples
Known GenesKRT75
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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