A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021371



Internal ID18763905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12490865..12670804hg38UCSC Ensembl
Innerchr7:12530491..12710429hg19UCSC Ensembl
Innerchr7:12497016..12676954hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38179940
hg19179939
hg18179939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6274n100
Supporting Variantsnssv3642977, nssv3642976
Samples
Known GenesSCIN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021371
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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