A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533655



Internal ID21858011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85017859..85017859hg38UCSC Ensembl
chr2:85244982..85244982hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045405
Supporting Variants
Samples
Known GenesKCMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533655
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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