A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010921



Internal ID19100138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:69683011..69716895hg38UCSC Ensembl
Innerchr1:70148694..70182578hg19UCSC Ensembl
Innerchr1:69921282..69955166hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3833885
hg1933885
hg1833885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n100
Supporting Variantsnssv3474727, nssv3701251
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)nsv1010921
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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