A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355202



Internal ID21012755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63317082..63372700hg38UCSC Ensembl
chr2:63544217..63599835hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3855619
hg1955619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089229
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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