A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054176



Internal ID19143395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107456259..107559672hg38UCSC Ensembl
Innerchr13:108108607..108212020hg19UCSC Ensembl
Innerchr13:106906608..107010021hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38103414
hg19103414
hg18103414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1740n100
Supporting Variantsnssv3525572, nssv3525571
Samples
Known GenesFAM155A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054176
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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