A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496772



Internal ID20869975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97519107..97523141hg38UCSC Ensembl
chr15:98062337..98066371hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384035
hg194035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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