A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342305



Internal ID20999858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20128814..20138170hg38UCSC Ensembl
chr2:20328575..20337931hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389357
hg199357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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