A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001651



Internal ID19090868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104201573..104687191hg38UCSC Ensembl
Innerchr3:103920417..104406035hg19UCSC Ensembl
Innerchr3:105403107..105888725hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38485619
hg19485619
hg18485619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604382
Samples
Known GenesMIR548A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001651
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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