A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605237



Internal ID20978308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77641392..77676965hg38UCSC Ensembl
chr7:77270709..77306282hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3835574
hg1935574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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