A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521418



Internal ID20894779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63201265..63201665hg38UCSC Ensembl
chr17:61278626..61279026hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037225
Samples
Known GenesTANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521418
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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