A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6769551



Internal ID10176079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:36957932..36959623hg38UCSC Ensembl
Outerchr1:37423533..37425224hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381692
hg191692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2747041, esv2747063, esv2747018, esv2747085
Supporting Variants
SamplesSSM065
Known GenesGRIK3
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)essv6769551
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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