A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603064



Internal ID20976135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21702257..21882540hg38UCSC Ensembl
chr7:21741875..21922158hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38180284
hg19180284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228198
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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