A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605435



Internal ID20978506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98733960..98735125hg38UCSC Ensembl
chr7:98363272..98364437hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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