A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341301



Internal ID20998854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149599685..150204988hg38UCSC Ensembl
chr2:150456199..151061502hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38605304
hg19605304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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