A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109524



Internal ID20676564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146808761..146809939hg38UCSC Ensembl
chr4:147729913..147731091hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381188
Supporting Variants
Samples
Known GenesTTC29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06884


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