A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998176



Internal ID19157713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75590743hg38UCSC Ensembl
Innerchr3:75469493..75639894hg19UCSC Ensembl
Innerchr3:75552183..75722584hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38170402
hg19170402
hg18170402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4784n100
Supporting Variantsnssv3596152, nssv3596145, nssv3596146, nssv3596149, nssv3596148, nssv3596151, nssv3596147, nssv3596150
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998176
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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