A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409922



Internal ID22467792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144850262..144868830hg38UCSC Ensembl
chr6:145171398..145189966hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3818569
hg1918569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891684
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409922
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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