A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344324



Internal ID21001877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150326917..150327116hg38UCSC Ensembl
chr2:151183431..151183630hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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