A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988700



Internal ID12629090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46412754..46572023hg38UCSC Ensembl
Innerchr10:46977594..47136994hg19UCSC Ensembl
Innerchr10:46397600..46557000hg18UCSC Ensembl
Innerchr10:46397600..46557000hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38159270
hg19159401
hg18159401
hg17159401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750903
Supporting Variants
SamplesBEC_613
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)essv6988700
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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