A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610992



Internal ID20984063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24569301..24572900hg38UCSC Ensembl
chr7:24608920..24612519hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610992
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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