A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431178



Internal ID21088731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142246057..142246483hg38UCSC Ensembl
chr7:141945876..141946302hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152410
Samples
Known GenesMOXD2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431178
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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