A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457246



Internal ID21114799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62431931..62461145hg38UCSC Ensembl
chr11:62199403..62228617hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3829215
hg1929215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993201
Samples
Known GenesAHNAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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