A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894974



Internal ID22670051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146944375..146945443hg38UCSC Ensembl
chr4:147865527..147866595hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419099
Samples
Known GenesTTC29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894974
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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