A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6620035



Internal ID20993106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97288370..97290004hg38UCSC Ensembl
chr7:96917682..96919316hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6620035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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