A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606739



Internal ID20979810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66528542..66577833hg38UCSC Ensembl
chr7:65993529..66042820hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3849292
hg1949292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158012
Samples
Known GenesLOC493754
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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