A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296101



Internal ID20505319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16032248..16046349hg38UCSC Ensembl
chr1:16358743..16372844hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814102
hg1914102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731176
Supporting Variants
Samples
Known GenesCLCNKA, CLCNKB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296101
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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