A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614780



Internal ID20987851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96685101..96686700hg38UCSC Ensembl
chr7:96314413..96316012hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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