A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624995



Internal ID6665155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132503737..132548845hg38UCSC Ensembl
chr10:134317241..134362349hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3845109
hg1945109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13983074
SamplesHG00096
Known GenesINPP5A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624995
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer