A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603043



Internal ID20976114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99742960..99743371hg38UCSC Ensembl
chr7:99340583..99340994hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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