A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007349



Internal ID19096568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130044843..130100783hg38UCSC Ensembl
Innerchr3:129763686..129819626hg19UCSC Ensembl
Innerchr3:131246376..131302316hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3855941
hg1955941
hg1855941
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4869n100
Supporting Variantsnssv3602798, nssv3602792, nssv3602790, nssv3602799, nssv3602796, nssv3602794, nssv3602791, nssv3602793, nssv3602789, nssv3602797, nssv3602795, nssv3735912
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007349
Frequency
Sample Size11257
Observed Gain9
Observed Loss3
Observed Complex0
Frequencyn/a


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