A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041764



Internal ID19130983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80619301..80681287hg38UCSC Ensembl
Innerchr9:83234216..83296202hg19UCSC Ensembl
Innerchr9:82424036..82486022hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3861987
hg1961987
hg1861987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697517
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)nsv1041764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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