A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355073



Internal ID21012626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67677201..67680800hg38UCSC Ensembl
chr2:67904333..67907932hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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