A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522848



Internal ID20896209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78505942..78589701hg38UCSC Ensembl
chr17:76502024..76585783hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3883760
hg1983760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038105
Samples
Known GenesDNAH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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