A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442149



Internal ID21099702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8759824..8765692hg38UCSC Ensembl
chr11:8781371..8787239hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385869
hg195869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994963
Samples
Known GenesST5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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