A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981030



Internal ID12972695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7425903..7532333hg38UCSC Ensembl
InnerchrX:7343944..7450374hg19UCSC Ensembl
InnerchrX:7353944..7460374hg18UCSC Ensembl
InnerchrX:7203680..7310110hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38106431
hg19106431
hg18106431
hg17106431
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)essv6981030
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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