A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500420



Internal ID20873647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17921465..17923090hg38UCSC Ensembl
chr17:17824779..17826404hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381626
hg191626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034108
Samples
Known GenesTOM1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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