A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435591



Internal ID21397593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95992472..95993270hg38UCSC Ensembl
chr8:97004700..97005498hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n172
Supporting Variantsnssv15754309
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435591
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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