A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29996



Internal ID12608190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:897556..2776199hg38UCSC Ensembl
InnerchrX:858291..2694240hg19UCSC Ensembl
InnerchrX:778291..2704240hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381878644
hg191835950
hg181925950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84235
SamplesHuRef
Known GenesAKAP17A, ASMT, ASMTL, ASMTL-AS1, CD99, CD99P1, CRLF2, CSF2RA, DHRSX, IL3RA, LINC00102, MIR3690, MIR3690-2, MIR6089-1, MIR6089-2, P2RY8, SLC25A6, XG, XGPY2, ZBED1
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29996
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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