A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603956



Internal ID20977027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69551585..69553941hg38UCSC Ensembl
chr7:69016571..69018927hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg382357
hg192357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603956
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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