A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048531



Internal ID19137750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29271508..29308144hg38UCSC Ensembl
Innerchr10:29560437..29597073hg19UCSC Ensembl
Innerchr10:29600443..29637079hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3836637
hg1936637
hg1836637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518207
Samples
Known GenesLYZL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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