A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6550882



Internal ID9328836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54564552..54565965hg38UCSC Ensembl
OuterchrX:54564513..54566022hg38UCSC Ensembl
InnerchrX:54590985..54592398hg19UCSC Ensembl
OuterchrX:54590946..54592455hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675067
Supporting Variants
SamplesNA18522
Known GenesGNL3L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6550882
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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