A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009168



Internal ID19098386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665198..94687282hg38UCSC Ensembl
Innerchr1:95130754..95152838hg19UCSC Ensembl
Innerchr1:94903342..94925426hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822085
hg1922085
hg1822085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3470145, nssv3467842
Samples
Known GenesLINC01057
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009168
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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