A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987933



Internal ID12626370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7904863..7983663hg38UCSC Ensembl
InnerchrX:7872904..7951704hg19UCSC Ensembl
InnerchrX:7832904..7911704hg18UCSC Ensembl
InnerchrX:7682640..7761440hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3878801
hg1978801
hg1878801
hg1778801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752336
Supporting Variants
SamplesBEC_374
Known GenesPNPLA4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987933
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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