A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416082



Internal ID21073635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143507716..143509600hg38UCSC Ensembl
chr7:143204809..143206693hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381885
hg191885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152491
Samples
Known GenesEPHA1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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