A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011472



Internal ID18754006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175044029..175073749hg38UCSC Ensembl
Innerchr1:175013165..175042885hg19UCSC Ensembl
Innerchr1:173279788..173309508hg18UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3829721
hg1929721
hg1829721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3491984
Samples
Known GenesTNN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011472
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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