A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002331



Internal ID19091548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:88493843..88584211hg38UCSC Ensembl
Innerchr1:88959526..89049894hg19UCSC Ensembl
Innerchr1:88732114..88822482hg18UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3890369
hg1990369
hg1890369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3481352
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)nsv1002331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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