A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020903



Internal ID21930246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64199284..64199465hg38UCSC Ensembl
chr11:63966756..63966937hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577895
Samples
Known GenesSTIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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