A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032906



Internal ID18775440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45101631..45245126hg38UCSC Ensembl
Innerchr6:45069368..45212863hg19UCSC Ensembl
Innerchr6:45177346..45320841hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38143496
hg19143496
hg18143496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745480
Samples
Known GenesMIR586, SUPT3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032906
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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