A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528990



Internal ID15456283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99523553..99524609hg38UCSC Ensembl
Innerchr6:99971429..99972485hg19UCSC Ensembl
Innerchr6:100078150..100079206hg18UCSC Ensembl
Innerchr6:100078150..100079206hg17UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381057
hg191057
hg181057
hg171057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv390n21
Supporting Variantsnssv705692
Samples
Known GenesTSTD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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