A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515737



Internal ID20889098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3771390..3781559hg38UCSC Ensembl
chr18:3771390..3781559hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3810170
hg1910170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040459
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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