A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450192



Internal ID21107745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30558777..30563114hg38UCSC Ensembl
chr11:30580324..30584661hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg384338
hg194338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990341
Samples
Known GenesMPPED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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