A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749948



Internal ID10330918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:81129540..81130251hg38UCSC Ensembl
Outerchr15:81421881..81422592hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6971283, essv6901725, essv6842884, essv6749993, essv6752874, essv6741598, essv6974851, essv6837876, essv6732541, essv6857902, essv6788201, essv6665361, essv6741455, essv6966498, essv6772505, essv6755901, essv6728718, essv6905319, essv6953697
SamplesSSM027, SSM046, SSM065, SSM087, SSM013, SSM057, SSM058, SSM028, SSM084, SSM047, SSM069, SSM029, SSM007, SSM010, SSM025, SSM004, SSM052, SSM056, SSM012
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2749948
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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