A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001697



Internal ID18744228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:171589803..171775069hg38UCSC Ensembl
Innerchr3:171307593..171492859hg19UCSC Ensembl
Innerchr3:172790287..172975553hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38185267
hg19185267
hg18185267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612702
Samples
Known GenesPLD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001697
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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