A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529396



Internal ID20902757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8402589..8404186hg38UCSC Ensembl
chr18:8402587..8404184hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044103
Samples
Known GenesPTPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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