A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6404259



Internal ID9506703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101087261..101093597hg38UCSC Ensembl
OuterchrX:101087224..101093647hg38UCSC Ensembl
InnerchrX:100342250..100348586hg19UCSC Ensembl
OuterchrX:100342213..100348636hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386424
hg196424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673239
Supporting Variants
SamplesNA18986
Known GenesTMEM35
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6404259
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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