A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535283



Internal ID20908644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13906401..13911700hg38UCSC Ensembl
chr18:13906400..13911699hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039241
Samples
Known GenesMC2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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