A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504616



Internal ID20877878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36534942..36548948hg38UCSC Ensembl
chr15:36827143..36841149hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3814007
hg1914007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504616
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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