A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502914



Internal ID20876163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44102121..44106473hg38UCSC Ensembl
chr17:42179489..42183841hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035756
Samples
Known GenesHDAC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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