A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497671



Internal ID20870879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42592732..42598266hg38UCSC Ensembl
chr15:42884930..42890464hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg385535
hg195535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023951
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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