A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522592



Internal ID18474187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46568009..46878295hg38UCSC Ensembl
Innerchr10:46674168..46981608hg19UCSC Ensembl
Innerchr10:46094174..46401614hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38310287
hg19307441
hg18307441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042820
Supporting Variants
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522592
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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