A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008984



Internal ID19098202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68669724..68698250hg38UCSC Ensembl
Innerchr3:68718875..68747401hg19UCSC Ensembl
Innerchr3:68801565..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3828527
hg1928527
hg1828527
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4771n100
Supporting Variantsnssv3732976, nssv3593997, nssv3593994, nssv3594001, nssv3593999, nssv3594002, nssv3593992, nssv3594007, nssv3593991, nssv3594009, nssv3593993, nssv3594005, nssv3593996, nssv3594003, nssv3594004, nssv3593995, nssv3594006, nssv3594000, nssv3593990, nssv3593998, nssv3594008
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008984
Frequency
Sample Size11257
Observed Gain2
Observed Loss19
Observed Complex0
Frequencyn/a


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