A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037157



Internal ID18779688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101283479..101386951hg38UCSC Ensembl
Innerchr9:104045761..104149233hg19UCSC Ensembl
Innerchr9:103085582..103189054hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38103473
hg19103473
hg18103473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697576
Samples
Known GenesBAAT, LPPR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037157
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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