A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015100



Internal ID19104317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105797939..105848082hg38UCSC Ensembl
Innerchr1:106340561..106390704hg19UCSC Ensembl
Innerchr1:106142084..106192227hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3850144
hg1950144
hg1850144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3498412
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)nsv1015100
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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