A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009719



Internal ID19098937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104402443..104485887hg38UCSC Ensembl
Innerchr1:104945065..105028509hg19UCSC Ensembl
Innerchr1:104746588..104830032hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3883445
hg1983445
hg1883445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486063, nssv3492813
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)nsv1009719
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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