A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513838



Internal ID20887187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43806775..43808361hg38UCSC Ensembl
chr15:44098973..44100559hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381587
hg191587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023997
Samples
Known GenesMFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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