A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264526



Internal ID20473744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:215007069..215007069hg38UCSC Ensembl
chr1:215180412..215180412hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761919
Supporting Variants
Samples
Known GenesKCNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264526
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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