A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549864



Internal ID16337273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4662517..4668106hg38UCSC Ensembl
Innerchr10:4704709..4710298hg19UCSC Ensembl
Innerchr10:4694709..4700298hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385590
hg195590
hg185590
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv742175, nssv742177, nssv742190, nssv742184, nssv742187, nssv742178, nssv742192, nssv742181, nssv742189, nssv742180, nssv742185, nssv742182, nssv742174, nssv742188, nssv742179, nssv742183, nssv742193, nssv742191, nssv742186, nssv742176
Samples
Known GenesLINC00704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549864
Frequency
Sample Size17421
Observed Gain13
Observed Loss7
Observed Complex0
Frequencyn/a


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