A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345982



Internal ID21003535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65351101..65407200hg38UCSC Ensembl
chr2:65578235..65634334hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3856100
hg1956100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089967
Samples
Known GenesSPRED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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