A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605433



Internal ID20978504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38792510..38794957hg38UCSC Ensembl
chr7:38832110..38834557hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382448
hg192448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156546
Samples
Known GenesVPS41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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