A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041651



Internal ID19130870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1989702..2021507hg38UCSC Ensembl
Innerchr10:2031896..2063701hg19UCSC Ensembl
Innerchr10:2021896..2053701hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3831806
hg1931806
hg1831806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3488602
Samples
Known GenesLINC00700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041651
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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