A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898818



Internal ID22673940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94656283..94656345hg38UCSC Ensembl
chr5:93991988..93992050hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416324
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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