A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984091



Internal ID12630979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46412752..46572051hg38UCSC Ensembl
Innerchr10:46977566..47136996hg19UCSC Ensembl
Innerchr10:46397572..46557002hg18UCSC Ensembl
Innerchr10:46397572..46557002hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159300
hg19159431
hg18159431
hg17159431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750905
Supporting Variants
SamplesBEC_77
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984091
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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