A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003697



Internal ID19092915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34625845..34638783hg38UCSC Ensembl
Innerchr1:35091446..35104384hg19UCSC Ensembl
Innerchr1:34864033..34876971hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812939
hg1912939
hg1812939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv146n100
Supporting Variantsnssv3466523
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)nsv1003697
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