A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610405



Internal ID20983476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21514803..21647576hg38UCSC Ensembl
chr7:21554421..21687194hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38132774
hg19132774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227836
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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