A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421177



Internal ID21078730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140405900..140406297hg38UCSC Ensembl
chr7:140105700..140106097hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150681
Samples
Known GenesRAB19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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