A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503704



Internal ID20876960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36625194..36636375hg38UCSC Ensembl
chr15:36917395..36928576hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811182
hg1911182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024351
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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