A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344383



Internal ID21001936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15144850..15148186hg38UCSC Ensembl
chr2:15284974..15288310hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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