A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505996



Internal ID20879271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31555979..31560380hg38UCSC Ensembl
chr17:29882998..29887399hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034898
Samples
Known GenesMIR193A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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