A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989283



Internal ID12974452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55994834..56263633hg38UCSC Ensembl
Innerchr10:57754594..58023394hg19UCSC Ensembl
Innerchr10:57424600..57693400hg18UCSC Ensembl
Innerchr10:57424600..57693400hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38268800
hg19268801
hg18268801
hg17268801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750966
Supporting Variants
SamplesBEC_520
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989283
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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