A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526719



Internal ID20900080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70094507..70101748hg38UCSC Ensembl
chr18:67761743..67768984hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg387242
hg197242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043678
Samples
Known GenesRTTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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