A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404371



Internal ID21061924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70665401..70672100hg38UCSC Ensembl
chr6:71375104..71381803hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230943
Samples
Known GenesSMAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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