A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498058



Internal ID20871266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24197401..24296300hg38UCSC Ensembl
chr15:24442548..24541447hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3898900
hg1998900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2414n223
Supporting Variantsnssv18023003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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