A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498322



Internal ID20871532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71111421..71340981hg38UCSC Ensembl
chr15:71403760..71633320hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38229561
hg19229561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026373
Samples
Known GenesCT62, THSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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