A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009143



Internal ID19098361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179013737..179066127hg38UCSC Ensembl
Innerchr3:178731525..178783915hg19UCSC Ensembl
Innerchr3:180214219..180266609hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3852391
hg1952391
hg1852391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614986
Samples
Known GenesZMAT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009143
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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