A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788235



Internal ID21233573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124471508..124471508hg38UCSC Ensembl
chr10:126160077..126160077hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677640
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788235
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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