A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009731



Internal ID19098949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:118657541..118677873hg38UCSC Ensembl
Innerchr1:119200164..119220496hg19UCSC Ensembl
Innerchr1:119001687..119022019hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3820333
hg1920333
hg1820333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv298n100
Supporting Variantsnssv3489405
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)nsv1009731
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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