A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024868



Internal ID19114085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122178920..122259649hg38UCSC Ensembl
Innerchr7:121818974..121899703hg19UCSC Ensembl
Innerchr7:121606210..121686939hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3880730
hg1980730
hg1880730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6603n100
Supporting Variantsnssv3662122
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)nsv1024868
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