A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922602



Internal ID22697827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132736003..132813784hg38UCSC Ensembl
chr10:134549507..134627288hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3877782
hg1977782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356506
Samples
Known GenesINPP5A, NKX6-2, TTC40
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922602
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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