A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603899



Internal ID20976970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73432301..73435800hg38UCSC Ensembl
chr7:72846631..72850130hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228966
Samples
Known GenesFZD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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