A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510558



Internal ID20883878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64389938..64392569hg38UCSC Ensembl
chr15:64682137..64684768hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025665
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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