A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052213



Internal ID18794744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95777038..95802184hg38UCSC Ensembl
Innerchr10:97536795..97561941hg19UCSC Ensembl
Innerchr10:97526785..97551931hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3825147
hg1925147
hg1825147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519046
Samples
Known GenesENTPD1, ENTPD1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052213
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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