A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897932



Internal ID22673042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4376934..4378882hg38UCSC Ensembl
chr4:4378661..4380609hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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