A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497608



Internal ID20870816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43993280..43994518hg38UCSC Ensembl
chr15:44285478..44286716hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381239
hg191239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024523
Samples
Known GenesFRMD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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