A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020849



Internal ID19110067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93892359..93943511hg38UCSC Ensembl
Innerchr5:93228065..93279216hg19UCSC Ensembl
Innerchr5:93253821..93304972hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3851153
hg1951152
hg1851152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5717n100
Supporting Variantsnssv3639937
Samples
Known GenesFAM172A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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