A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573263



Internal ID21765306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36681589..36681589hg38UCSC Ensembl
chr6:36649366..36649366hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076294
Supporting Variants
Samples
Known GenesCDKN1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573263
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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