A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013973



Internal ID21923316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96349320..96349519hg38UCSC Ensembl
chr9:99111602..99111801hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597182
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013973
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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