A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6249720



Internal ID9800804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:68012440..68026378hg38UCSC Ensembl
OuterchrX:68012403..68026428hg38UCSC Ensembl
InnerchrX:67232282..67246220hg19UCSC Ensembl
OuterchrX:67232245..67246270hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3814026
hg1914026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671916
Supporting Variants
SamplesNA19835
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6249720
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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