A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3499073



Internal ID18740028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:177913037..177958519hg38UCSC Ensembl
Innerchr1:177882172..177927654hg19UCSC Ensembl
Innerchr1:176148795..176194277hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3845483
hg1945483
hg1845483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010839
Supporting Variants
Samples
Known GenesSEC16B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3499073
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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