A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv806n100



Internal ID20152422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46441715..46489856hg38UCSC Ensembl
chr10:47055642..47108045hg19UCSC Ensembl
chr10:46475648..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3848142
hg1952404
hg1852404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050844, nsv1039572, nsv1047314, nsv1047841, nsv1053661, nsv1042132, nsv1048581, nsv1050085, nsv1053113, nsv1041715, nsv1050998
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv806n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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