A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496732



Internal ID20869935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43989879..44128614hg38UCSC Ensembl
chr15:44282077..44420812hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38138736
hg19138736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024556
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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