A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497078



Internal ID20870282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56370901..56541500hg38UCSC Ensembl
chr15:56663099..56833698hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38170600
hg19170600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2548n223
Supporting Variantsnssv18024898
Samples
Known GenesMNS1, TEX9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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