A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011898



Internal ID18754433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78308939..78350115hg38UCSC Ensembl
Innerchr1:78774623..78815799hg19UCSC Ensembl
Innerchr1:78547211..78588387hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841177
hg1941177
hg1841177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3699590
Samples
Known GenesMGC27382
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011898
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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