A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617014



Internal ID20990085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77232166..77232854hg38UCSC Ensembl
chr7:76861483..76862171hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160212
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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