A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603815



Internal ID20976886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12698811..12699568hg38UCSC Ensembl
chr7:12738436..12739193hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603815
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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