A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473187



Internal ID21130740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77231779..77232217hg38UCSC Ensembl
chr11:76942824..76943262hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994133
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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