A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987898



Internal ID12972690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7425907..7532331hg38UCSC Ensembl
InnerchrX:7343948..7450372hg19UCSC Ensembl
InnerchrX:7353948..7460372hg18UCSC Ensembl
InnerchrX:7203684..7310108hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38106425
hg19106425
hg18106425
hg17106425
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987898
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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