A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030442



Internal ID19119661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60591828..61103618hg38UCSC Ensembl
Innerchr6:57559575..58071365hg19UCSC Ensembl
Innerchr6:57667534..58179324hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38511791
hg19511791
hg18511791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5971n100
Supporting Variantsnssv3745506
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)nsv1030442
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