A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176906



Internal ID20743946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128744149..128744731hg38UCSC Ensembl
chr9:131506428..131507010hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446086
Supporting Variants
Samples
Known GenesZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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