A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522158



Internal ID20895519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78170417..78170701hg38UCSC Ensembl
chr17:76166498..76166782hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038082
Samples
Known GenesSYNGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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