A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042678



Internal ID21951990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19931966..19931966hg38UCSC Ensembl
chr2:20131727..20131727hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535818
Samples
Known GenesWDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042678
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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