A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6685957



Internal ID9753506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:55032942..55033358hg38UCSC Ensembl
Outerchr19:55544310..55544726hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718937, esv2718872, esv2718941, esv2718938
Supporting Variants
SamplesSSM034
Known GenesGP6
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)essv6685957
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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