A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377595



Internal ID21035148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16851873..16903205hg38UCSC Ensembl
chr5:16851982..16903314hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3851333
hg1951333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129532
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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