A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615463



Internal ID20988534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53359134..53382301hg38UCSC Ensembl
chr7:53426827..53449994hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3823168
hg1923168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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