A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038358



Internal ID19127577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19030782..19055881hg38UCSC Ensembl
Innerchr10:19319711..19344810hg19UCSC Ensembl
Innerchr10:19359717..19384816hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3825100
hg1925100
hg1825100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv682n100
Supporting Variantsnssv3515410, nssv3521972, nssv3511139
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)nsv1038358
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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