A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604930



Internal ID20978001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73467024..73467667hg38UCSC Ensembl
chr7:72881354..72881997hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231243
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604930
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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