A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341120



Internal ID20998673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65801642..65802225hg38UCSC Ensembl
chr2:66028776..66029359hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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