A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013561



Internal ID19102779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:94665110..94689843hg38UCSC Ensembl
Innerchr1:95130666..95155399hg19UCSC Ensembl
Innerchr1:94903254..94927987hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824734
hg1924734
hg1824734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv208n100
Supporting Variantsnssv3480134, nssv3467050, nssv3472181, nssv3470435, nssv3471917, nssv3473967, nssv3470781, nssv3471529, nssv3479468, nssv3469198, nssv3464727, nssv3464554, nssv3482337, nssv3469044, nssv3480450, nssv3467056
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)nsv1013561
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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