A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv739n100



Internal ID19011107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46526513..46962260hg38UCSC Ensembl
chr10:46590219..47046997hg19UCSC Ensembl
chr10:46010225..46467003hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38435748
hg19456779
hg18456779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047173, nsv1039540, nsv1048873, nsv1048798, nsv1051263, nsv1038461, nsv1035646, nsv1045619, nsv1035164, nsv1054516
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv739n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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