A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349732



Internal ID21007285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67057688..67058261hg38UCSC Ensembl
chr2:67284820..67285393hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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