A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601432



Internal ID20974503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33724685..33733091hg38UCSC Ensembl
chr7:33764297..33772703hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg388407
hg198407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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