A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981031



Internal ID12972696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7436306..7540555hg38UCSC Ensembl
InnerchrX:7354347..7458596hg19UCSC Ensembl
InnerchrX:7364347..7468596hg18UCSC Ensembl
InnerchrX:7214083..7318332hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38104250
hg19104250
hg18104250
hg17104250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752333
Supporting Variants
SamplesBEC_341
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981031
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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