A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619073



Internal ID20992144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51155601..51164600hg38UCSC Ensembl
chr7:51223298..51232297hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234733
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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