A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012503



Internal ID18755036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16931632hg38UCSC Ensembl
Innerchr1:17177033..17258127hg19UCSC Ensembl
Innerchr1:17049620..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3881095
hg1981095
hg1881095
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3481474, nssv3469981, nssv3463579, nssv3469359, nssv3479388, nssv3463175, nssv3481448
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012503
Frequency
Sample Size29084
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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