A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039523



Internal ID19128742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130058109..130097459hg38UCSC Ensembl
Innerchr10:131856373..131895723hg19UCSC Ensembl
Innerchr10:131746363..131785713hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3839351
hg1939351
hg1839351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506012
Samples
Known GenesLINC00959
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039523
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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