A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463414



Internal ID21120967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71501700..71504676hg38UCSC Ensembl
chr11:71212746..71215722hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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