A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608398



Internal ID20981469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95978351..95980855hg38UCSC Ensembl
chr7:95607663..95610167hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382505
hg192505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160690
Samples
Known GenesDYNC1I1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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