A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611252



Internal ID20984323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7473456..7561377hg38UCSC Ensembl
chr7:7513087..7601008hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3887922
hg1987922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159560
Samples
Known GenesCOL28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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