A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431229



Internal ID21088782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130315190..130322078hg38UCSC Ensembl
chr7:129955030..129961918hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg386889
hg196889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153429
Samples
Known GenesCPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431229
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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