A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988506



Internal ID12626681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:2504267..2776199hg38UCSC Ensembl
InnerchrX:2422308..2694240hg19UCSC Ensembl
InnerchrX:2432308..2704240hg18UCSC Ensembl
InnerchrX:2415669..2687601hg17UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38271933
hg19271933
hg18271933
hg17271933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752318
Supporting Variants
SamplesBEC_402
Known GenesCD99, CD99P1, LINC00102, MIR6089-1, MIR6089-2, XG, XGPY2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988506
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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