A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422994



Internal ID22480864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39537546..39538245hg38UCSC Ensembl
chr4:39539166..39539865hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889408
Supporting Variants
Samples
Known GenesMIR1273H, UGDH-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422994
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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