A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750095



Internal ID21385756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88064283..88065282hg38UCSC Ensembl
chr6:88774001..88775000hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435043
Supporting Variants
SamplesMDQ010
Known GenesSPACA1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750095
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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