A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504749



Internal ID20878012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40379813..40384285hg38UCSC Ensembl
chr15:40672014..40676486hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384473
hg194473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024519
Samples
Known GenesKNSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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