A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002522



Internal ID19091739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79745013..80066448hg38UCSC Ensembl
Innerchr1:80210698..80532133hg19UCSC Ensembl
Innerchr1:79983286..80304721hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38321436
hg19321436
hg18321436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv203n100
Supporting Variantsnssv3699592
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)nsv1002522
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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