A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588131



Internal ID21780174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132569925..132570072hg38UCSC Ensembl
chr10:134383429..134383576hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032608
Supporting Variants
Samples
Known GenesINPP5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588131
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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