A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749634



Internal ID21389662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95992473..95993271hg38UCSC Ensembl
chr8:97004701..97005499hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435592
Supporting Variants
SamplesNB10
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749634
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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