A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030088



Internal ID19119307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137062008..137108951hg38UCSC Ensembl
Innerchr6:137383145..137430088hg19UCSC Ensembl
Innerchr6:137424838..137471781hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3846944
hg1946944
hg1846944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6151n100
Supporting Variantsnssv3654411
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)nsv1030088
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer