A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044018



Internal ID21953309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68978271..68978271hg38UCSC Ensembl
chr2:69205403..69205403hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534440
Samples
Known GenesGKN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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