A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751849



Internal ID15699119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79935003..79940225hg38UCSC Ensembl
Innerchr10:81694759..81699981hg19UCSC Ensembl
Innerchr10:81684739..81689961hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385223
hg195223
hg185223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551636
Supporting Variants
Samples
Known GenesSFTPD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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