A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603722



Internal ID20976793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29076144..29088009hg38UCSC Ensembl
chr7:29115760..29127625hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3811866
hg1911866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237077
Samples
Known GenesCPVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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