A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035358



Internal ID19124577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105922473..105963481hg38UCSC Ensembl
Innerchr10:107682231..107723239hg19UCSC Ensembl
Innerchr10:107672221..107713229hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3841009
hg1941009
hg1841009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503666
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)nsv1035358
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