A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017724



Internal ID19106941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76730151..76758737hg38UCSC Ensembl
Innerchr6:77439868..77468454hg19UCSC Ensembl
Innerchr6:77496587..77525173hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3828587
hg1928587
hg1828587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6021n100
Supporting Variantsnssv3659041
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)nsv1017724
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