A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353751



Internal ID21011304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219869505..219870276hg38UCSC Ensembl
chr2:220734226..220734997hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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