A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046901



Internal ID19136120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37504203..37540973hg38UCSC Ensembl
Innerchr13:38078340..38115110hg19UCSC Ensembl
Innerchr13:36976340..37013110hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3836771
hg1936771
hg1836771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1628n100
Supporting Variantsnssv3523332, nssv3523333, nssv3523334, nssv3523331, nssv3523329, nssv3523336, nssv3523335, nssv3523330
Samples
Known GenesLINC00547
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046901
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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