A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037395



Internal ID18779926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526513..46878295hg38UCSC Ensembl
Innerchr10:46674168..47047587hg19UCSC Ensembl
Innerchr10:46094174..46467593hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38351783
hg19373420
hg18373420
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv740n100
Supporting Variantsnssv3503785, nssv3511198, nssv3520874, nssv3707845, nssv3521140, nssv3504507, nssv3510432
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037395
Frequency
Sample Size29084
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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