A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978891



Internal ID12979316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20016665..20030965hg38UCSC Ensembl
Innerchr10:20305594..20319894hg19UCSC Ensembl
Innerchr10:20345600..20359900hg18UCSC Ensembl
Innerchr10:20345600..20359900hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3814301
hg1914301
hg1814301
hg1714301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34798
Supporting Variants
SamplesNA12760
Known GenesPLXDC2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978891
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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