A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029002



Internal ID19118221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76731101..76758909hg38UCSC Ensembl
Innerchr6:77440818..77468626hg19UCSC Ensembl
Innerchr6:77497537..77525345hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3827809
hg1927809
hg1827809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3659049
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)nsv1029002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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