A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596361



Internal ID6983678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61833732..61870619hg38UCSC Ensembl
chr3:61819406..61856293hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3836888
hg1936888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026198
SamplesHG02277
Known GenesPTPRG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596361
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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