A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042995



Internal ID19132214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121673138..121702140hg38UCSC Ensembl
Innerchr10:123432652..123461654hg19UCSC Ensembl
Innerchr10:123422642..123451644hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829003
hg1929003
hg1829003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3514660
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)nsv1042995
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