A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038952



Internal ID18781483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46962260hg38UCSC Ensembl
Innerchr10:46590219..47058976hg19UCSC Ensembl
Innerchr10:46010225..46478982hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38435748
hg19468758
hg18468758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv737n100
Supporting Variantsnssv3506912
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)nsv1038952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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