A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606681



Internal ID20979752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17346507..17590170hg38UCSC Ensembl
chr7:17386131..17629794hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38243664
hg19243664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606681
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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