A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433933



Internal ID21091486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130379701..130382100hg38UCSC Ensembl
chr7:130019542..130021941hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153432
Samples
Known GenesCPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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