A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343551



Internal ID21001104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238713849..238714927hg38UCSC Ensembl
chr2:239622490..239623568hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343551
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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