A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046521



Internal ID19135740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70161932..70198751hg38UCSC Ensembl
Innerchr13:70736064..70772883hg19UCSC Ensembl
Innerchr13:69634065..69670884hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3836820
hg1936820
hg1836820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1712n100
Supporting Variantsnssv3713219, nssv3529297, nssv3529306, nssv3529295, nssv3713210, nssv3529298, nssv3529310, nssv3713211, nssv3529303, nssv3529299, nssv3713220, nssv3529314, nssv3529309, nssv3529307, nssv3713216, nssv3529318, nssv3713214, nssv3529302, nssv3529316, nssv3713212, nssv3529301, nssv3529304, nssv3529296, nssv3713208, nssv3529311, nssv3529315, nssv3529313, nssv3713206, nssv3713217, nssv3713221, nssv3713224, nssv3713215, nssv3713223, nssv3529317, nssv3529308, nssv3713222, nssv3713218, nssv3529305, nssv3713213, nssv3713209, nssv3529319, nssv3529312, nssv3713207, nssv3529300
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046521
Frequency
Sample Size11257
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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