A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619736



Internal ID20992807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51203205..51203475hg38UCSC Ensembl
chr7:51270902..51271172hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157612
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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