A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15754117



Internal ID21384231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374556..39529709hg38UCSC Ensembl
chr8:39232075..39387228hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155154
hg19155154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435496
Supporting Variants
SamplesBTQ016
Known GenesADAM3A, ADAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15754117
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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