A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608999



Internal ID20982070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:70343301..70393700hg38UCSC Ensembl
chr7:69808287..69858686hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3850400
hg1950400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158649
Samples
Known GenesAUTS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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