A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054197



Internal ID19143416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122874701..122916819hg38UCSC Ensembl
Innerchr10:124634217..124676335hg19UCSC Ensembl
Innerchr10:124624207..124666325hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3842119
hg1942119
hg1842119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516588
Samples
Known GenesFAM24A, FAM24B, FAM24B-CUZD1, LOC399815
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054197
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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