A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510985



Internal ID20884309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67599580..67599967hg38UCSC Ensembl
chr15:67891918..67892305hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025467
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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