A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038585



Internal ID18781116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46481242hg38UCSC Ensembl
Innerchr10:47068215..47138582hg19UCSC Ensembl
Innerchr10:46488221..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3870073
hg1970368
hg1870368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv813n100
Supporting Variantsnssv3508289, nssv3705908
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038585
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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