A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519734



Internal ID20893095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76564368..76577863hg38UCSC Ensembl
chr17:74560450..74573945hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3813496
hg1913496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196622
Samples
Known GenesSNHG16, ST6GALNAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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