A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505197



Internal ID20878463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75630721..75644207hg38UCSC Ensembl
chr15:75923062..75936548hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3813487
hg1913487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2586n223
Supporting Variantsnssv18025735
Samples
Known GenesIMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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