A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487814



Internal ID265144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157013341..157013428hg38UCSC Ensembl
chr7:156806035..156806122hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005996
Samples
Known GenesMNX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487814
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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