A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503644



Internal ID20876900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35783641..35784154hg38UCSC Ensembl
chr15:36075842..36076355hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023438
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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