A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529947



Internal ID20903308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39635203..39692930hg38UCSC Ensembl
chr18:37215167..37272894hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3857728
hg1957728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040186
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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