A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521085



Internal ID20894446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50231101..50236200hg38UCSC Ensembl
chr18:47757471..47762570hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042179
Samples
Known GenesCCDC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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