A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010626



Internal ID18753158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186838983..186859338hg38UCSC Ensembl
Innerchr3:186556772..186577127hg19UCSC Ensembl
Innerchr3:188039466..188059821hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3820356
hg1920356
hg1820356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615035
Samples
Known GenesADIPOQ, ADIPOQ-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010626
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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