A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047555



Internal ID21956789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61137697..61137697hg38UCSC Ensembl
chr2:61364832..61364832hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526656
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047555
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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