A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2741695



Internal ID10295811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:7498707..7498913hg38UCSC Ensembl
Outerchr1:7558767..7558973hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6925676
SamplesSSM019
Known GenesCAMTA1
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)esv2741695
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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