A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221548



Internal ID20788588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69621285..69699300hg38UCSC Ensembl
chr6:70331177..70409192hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3878016
hg1978016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407965
Supporting Variants
Samples
Known GenesLMBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221548
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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