A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517801



Internal ID20891162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61373701..61375800hg38UCSC Ensembl
chr17:59451062..59453161hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037090
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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