A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412759



Internal ID22470629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36468282..36468614hg38UCSC Ensembl
chr4:36469904..36470236hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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