A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486399



Internal ID19074040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106657722..106692505hg38UCSC Ensembl
Innerchr1:107200344..107235127hg19UCSC Ensembl
Innerchr1:107001867..107036650hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3834784
hg1934784
hg1834784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003608
Supporting Variants
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)nssv3486399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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