A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615583



Internal ID20988654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28539299..28551289hg38UCSC Ensembl
chr7:28578917..28590907hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3811991
hg1911991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157086
Samples
Known GenesCREB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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