A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614179



Internal ID20987250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46621301..46622400hg38UCSC Ensembl
chr7:46660899..46661998hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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