A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430567



Internal ID21088120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140399704..140408305hg38UCSC Ensembl
chr7:140099504..140108105hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg388602
hg198602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150679
Samples
Known GenesRAB19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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