A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601606



Internal ID20974677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33123875..33598492hg38UCSC Ensembl
chr7:33163487..33638104hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38474618
hg19474618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224242
Samples
Known GenesBBS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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