A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609779



Internal ID20982850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100114681..100116601hg38UCSC Ensembl
chr7:99712304..99714224hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381921
hg191921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147681
Samples
Known GenesTAF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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