A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342112



Internal ID20999665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145094776..145161245hg38UCSC Ensembl
chr2:145852343..145918812hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3866470
hg1966470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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