A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473020



Internal ID21130573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74026747..74027189hg38UCSC Ensembl
chr11:73737792..73738234hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993897
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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