A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026176



Internal ID18768708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151621328..151688239hg38UCSC Ensembl
Innerchr5:151000889..151067800hg19UCSC Ensembl
Innerchr5:150981082..151047993hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3866912
hg1966912
hg1866912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648175
Samples
Known GenesSPARC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026176
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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