A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624139



Internal ID6664306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88724980..89003307hg38UCSC Ensembl
chr10:90484737..90763064hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38278328
hg19278328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13890207
SamplesHG02309
Known GenesACTA2, ANKRD22, FAS, FAS-AS1, LIPK, LIPM, LIPN, STAMBPL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624139
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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