A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615321



Internal ID20988392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74199194..74200185hg38UCSC Ensembl
chr7:73613524..73614515hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615321
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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