A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013869



Internal ID18756401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41121740..41174077hg38UCSC Ensembl
Innerchr1:41587412..41639749hg19UCSC Ensembl
Innerchr1:41359999..41412336hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3852338
hg1952338
hg1852338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3477086
Samples
Known GenesMIR5095, SCMH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013869
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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