A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828996



Internal ID22603931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202158997..202182740hg38UCSC Ensembl
chr1:202128125..202151868hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3823744
hg1923744
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457128
Samples
Known GenesPTPN7, PTPRVP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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