A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500983



Internal ID20874213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88371234..88374237hg38UCSC Ensembl
chr15:88914465..88917468hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383004
hg193004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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