A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014462



Internal ID21923805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142657213..142796373hg38UCSC Ensembl
chr7:142364710..142494057hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38139161
hg19129348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571858
Samples
Known GenesMTRNR2L6, PRSS1, PRSS2, PRSS3P2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014462
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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