A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609787



Internal ID20982858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54072722..54074414hg38UCSC Ensembl
chr7:54140415..54142107hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg381693
hg191693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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