A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514242



Internal ID20887594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56401833..56566829hg38UCSC Ensembl
chr15:56694031..56859027hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38164997
hg19164997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2548n223
Supporting Variantsnssv18025315
Samples
Known GenesMNS1, TEX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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