A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526500



Internal ID20899861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58647945..58689459hg38UCSC Ensembl
chr17:56725306..56766820hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3841515
hg1941515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036313
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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