A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670601



Internal ID9590020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155532655..155548549hg38UCSC Ensembl
OuterchrX:155532618..155548599hg38UCSC Ensembl
InnerchrX:154762316..154778210hg19UCSC Ensembl
OuterchrX:154762279..154778260hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3815982
hg1915982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6436487
SamplesNA19661
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670601
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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