A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407965



Internal ID21065518
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 StatusM
Merged Variants
Supporting Variantsnssv18221548
Samples
Known GenesLMBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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