A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986677



Internal ID12632226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6482582..6909654hg38UCSC Ensembl
InnerchrX:6400623..6827695hg19UCSC Ensembl
InnerchrX:6410623..6837695hg18UCSC Ensembl
InnerchrX:6260359..6687431hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38427073
hg19427073
hg18427073
hg17427073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35137
Supporting Variants
SamplesNA12057
Known GenesVCX3A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986677
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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