A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008562



Internal ID18751093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35954987..36032074hg38UCSC Ensembl
Innerchr1:36420588..36497675hg19UCSC Ensembl
Innerchr1:36193175..36270262hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3877088
hg1977088
hg1877088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv149n100
Supporting Variantsnssv3478127
Samples
Known GenesAGO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008562
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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