A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037576



Internal ID18780107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97031342..97113892hg38UCSC Ensembl
Innerchr10:98791099..98873649hg19UCSC Ensembl
Innerchr10:98781089..98863639hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3882551
hg1982551
hg1882551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv963n100
Supporting Variantsnssv3505112
Samples
Known GenesLOC100505540, SLIT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037576
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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