A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896919



Internal ID22672016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185240381..185240557hg38UCSC Ensembl
chr4:186161535..186161711hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417679
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896919
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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