A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048568



Internal ID19137787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121675623..121700627hg38UCSC Ensembl
Innerchr10:123435137..123460141hg19UCSC Ensembl
Innerchr10:123425127..123450131hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3825005
hg1925005
hg1825005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3518254
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)nsv1048568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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