A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002363



Internal ID19091580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104649483..104682708hg38UCSC Ensembl
Innerchr1:105192105..105225330hg19UCSC Ensembl
Innerchr1:104993628..105026853hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3833226
hg1933226
hg1833226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492513, nssv3497532
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)nsv1002363
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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