A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496187



Internal ID20869386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33063260..33069964hg38UCSC Ensembl
chr15:33355461..33362165hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg386705
hg196705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023569
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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