A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503639



Internal ID20876895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70193991..70196226hg38UCSC Ensembl
chr15:70486330..70488565hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382236
hg192236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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