A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415658



Internal ID21073211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155378153..155405535hg38UCSC Ensembl
chr7:155170848..155198230hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3827383
hg1927383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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