A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999722



Internal ID19159258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75636809hg38UCSC Ensembl
Innerchr3:75421158..75685960hg19UCSC Ensembl
Innerchr3:75503848..75768650hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38264803
hg19264803
hg18264803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3733027
Samples
Known GenesFAM86DP, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999722
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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