A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv765n100



Internal ID20152381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46332711..46606240hg38UCSC Ensembl
chr10:46943377..47249575hg19UCSC Ensembl
chr10:46363383..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38273530
hg19306199
hg18306199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039576, nsv1055049
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, GPRIN2, 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)dgv765n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer