A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037657



Internal ID18780188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:88570153..88608133hg38UCSC Ensembl
Innerchr10:90329910..90367890hg19UCSC Ensembl
Innerchr10:90319890..90357870hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3837981
hg1937981
hg1837981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505213
Samples
Known GenesLIPJ, RNLS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037657
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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