A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013397



Internal ID19102615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102187221..102387282hg38UCSC Ensembl
Innerchr1:102652777..102852838hg19UCSC Ensembl
Innerchr1:102425365..102625426hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38200062
hg19200062
hg18200062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n100
Supporting Variantsnssv3469715, nssv3699606, nssv3699608, nssv3474461, nssv3472185, nssv3699607, nssv3465936, nssv3472241, nssv3468689
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013397
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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