A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609497



Internal ID20982568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392587..66395177hg38UCSC Ensembl
chr7:65857574..65860164hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382591
hg192591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158002
Samples
Known GenesLINC00174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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