A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176957



Internal ID20743997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131160835..131161988hg38UCSC Ensembl
chr9:134036222..134037375hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381154
hg191154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444629
Supporting Variants
Samples
Known GenesNUP214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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