A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020060



Internal ID19109279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143733941..143850167hg38UCSC Ensembl
Innerchr7:143431034..143547260hg19UCSC Ensembl
Innerchr7:143061967..143178193hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38116227
hg19116227
hg18116227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6710n100
Supporting Variantsnssv3754750
Samples
Known GenesCTAGE6, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020060
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