A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616122



Internal ID20989193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33557900..33773435hg38UCSC Ensembl
chr7:33597512..33813047hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38215536
hg19215536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227333
Samples
Known GenesBBS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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