A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748946



Internal ID21386333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:993766..994765hg38UCSC Ensembl
chr6:994001..995000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435054
Supporting Variants
SamplesMDQ010
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748946
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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