A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024524



Internal ID19113741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:70566255..70673938hg38UCSC Ensembl
Innerchr7:70031241..70138924hg19UCSC Ensembl
Innerchr7:69669177..69776860hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38107684
hg19107684
hg18107684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755296
Samples
Known GenesAUTS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024524
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