A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451634



Internal ID21109187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113245327..113249645hg38UCSC Ensembl
chr9:116007607..116011925hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg384319
hg194319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174381
Samples
Known GenesSLC31A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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