A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861432



Internal ID22636367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155001779..155003882hg38UCSC Ensembl
chr7:154793489..154795592hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503382
Samples
Known GenesPAXIP1, PAXIP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861432
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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