A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3480982



Internal ID19069474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665950..94687706hg38UCSC Ensembl
Innerchr1:95131506..95153262hg19UCSC Ensembl
Innerchr1:94904094..94925850hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3821757
hg1921757
hg1821757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004829
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)nssv3480982
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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