A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049748



Internal ID19138967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109166226..109282250hg38UCSC Ensembl
Innerchr10:110925984..111042008hg19UCSC Ensembl
Innerchr10:110915974..111031998hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38116025
hg19116025
hg18116025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv973n100
Supporting Variantsnssv3706234, nssv3522044
Samples
Known GenesRNU6-53P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049748
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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