A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616309



Internal ID20989380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66396260..66408653hg38UCSC Ensembl
chr7:65861247..65873640hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3812394
hg1912394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158003
Samples
Known GenesLINC00174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616309
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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