A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003506



Internal ID19092724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:95577454..95599898hg38UCSC Ensembl
Innerchr1:96043010..96065454hg19UCSC Ensembl
Innerchr1:95815598..95838042hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822445
hg1922445
hg1822445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3466285
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)nsv1003506
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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