A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv764n100



Internal ID20152380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395843..46606240hg38UCSC Ensembl
chr10:46943377..47153919hg19UCSC Ensembl
chr10:46363383..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38210398
hg19210543
hg18210543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041317, nsv1051992, nsv1054689, nsv1049592, nsv1038574, nsv1047743, nsv1055122, nsv1045574, nsv1044209, nsv1038133
Samples
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv764n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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