A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406744



Internal ID21064297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95512608..95517720hg38UCSC Ensembl
chr5:94848312..94853424hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385113
hg195113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136525
Samples
Known GenesTTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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