A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864152



Internal ID22639087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131058276..131067826hg38UCSC Ensembl
chr7:130743035..130752585hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg389551
hg199551
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503936
Samples
Known GenesLINC-PINT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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