A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619481



Internal ID20992552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74178105..74186261hg38UCSC Ensembl
chr7:73592435..73600591hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388157
hg198157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159513
Samples
Known GenesEIF4H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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