A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003354



Internal ID19092573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94687706hg38UCSC Ensembl
Innerchr1:95130666..95153262hg19UCSC Ensembl
Innerchr1:94903254..94925850hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3822597
hg1922597
hg1822597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3467315, nssv3477861, nssv3469554, nssv3477740, nssv3474719, nssv3475654, nssv3480148, nssv3473952, nssv3466801, nssv3467100, nssv3465940, nssv3468354, nssv3480124, nssv3469757, nssv3466477, nssv3465935, nssv3475501
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)nsv1003354
Frequency
Sample Size11257
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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