A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677714



Internal ID9597133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111314868..111316106hg38UCSC Ensembl
chrX:110558096..110559334hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381239
hg191239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5797023, essv6475267, essv6076026, essv5470557, essv6118508, essv6381876, essv6078337, essv5990653, essv5539390, essv5472758, essv5517560, essv6172860, essv6568076, essv6163870, essv5581773, essv6298016, essv6477376, essv5974961, essv5946099, essv5499246, essv5668927, essv5485258, essv6345686, essv5766809
SamplesNA19701, NA19909, NA19393, NA19377, NA19315, NA19457, NA19313, NA18498, NA19917, NA19471, NA19189, NA19908, NA19437, NA19469, NA19108, NA19434, NA19473, NA19435, NA19331, NA19470, HG01342, NA19438, NA19463, NA19676
Known GenesDCX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677714
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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