A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3482483



Internal ID18723560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35949901..36003531hg38UCSC Ensembl
Innerchr1:36415502..36469132hg19UCSC Ensembl
Innerchr1:36188089..36241719hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3853631
hg1953631
hg1853631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009033
Supporting Variants
Samples
Known GenesAGO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3482483
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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