A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6281768



Internal ID9259171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:91758317..91819923hg38UCSC Ensembl
OuterchrX:91757946..91820293hg38UCSC Ensembl
InnerchrX:91013316..91074922hg19UCSC Ensembl
OuterchrX:91012945..91075292hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3862348
hg1962348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2656576
Supporting Variants
SamplesHG00403
Known GenesPCDH11X
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6281768
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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