A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048506



Internal ID19137725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121004150..121017973hg38UCSC Ensembl
Innerchr10:122763663..122777486hg19UCSC Ensembl
Innerchr10:122753653..122767476hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3813824
hg1913824
hg1813824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv978n100
Supporting Variantsnssv3510599, nssv3507928, nssv3503891, nssv3505919
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048506
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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