A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049740



Internal ID19138959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101287342..101313543hg38UCSC Ensembl
Innerchr9:104049624..104075825hg19UCSC Ensembl
Innerchr9:103089445..103115646hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3826202
hg1926202
hg1826202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759792
Samples
Known GenesLPPR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049740
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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