A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462609



Internal ID21120162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71443489..71446952hg38UCSC Ensembl
chr11:71154535..71157998hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992873
Samples
Known GenesDHCR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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