A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614161



Internal ID20987232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73861936..73862244hg38UCSC Ensembl
chr7:73276266..73276574hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228838
Samples
Known GenesWBSCR28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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