A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465617



Internal ID19061313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665129..94687282hg38UCSC Ensembl
Innerchr1:95130685..95152838hg19UCSC Ensembl
Innerchr1:94903273..94925426hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822154
hg1922154
hg1822154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010621
Supporting Variants
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)nssv3465617
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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