A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610885



Internal ID20983956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69086415..69098617hg38UCSC Ensembl
chr7:68551402..68563604hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3812203
hg1912203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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