A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013052



Internal ID19102270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104562716..104633369hg38UCSC Ensembl
Innerchr1:105105338..105175991hg19UCSC Ensembl
Innerchr1:104906861..104977514hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3870654
hg1970654
hg1870654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv232n100
Supporting Variantsnssv3494051
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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