A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428314



Internal ID21085867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157613691..157615925hg38UCSC Ensembl
chr7:157406383..157408617hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151542
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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