A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440030



Internal ID21097583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30562332..30562894hg38UCSC Ensembl
chr11:30583879..30584441hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990343
Samples
Known GenesMPPED2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440030
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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