A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510300



Internal ID20883617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62663348..62664866hg38UCSC Ensembl
chr15:62955547..62957065hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381519
hg191519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025600
Samples
Known GenesTLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510300
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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