A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008362



Internal ID19097580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120182927..120200823hg38UCSC Ensembl
Innerchr3:119901774..119919670hg19UCSC Ensembl
Innerchr3:121384464..121402360hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3817897
hg1917897
hg1817897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604521, nssv3604520
Samples
Known GenesGPR156
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008362
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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