A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842830



Internal ID16136786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49252812..49265736hg38UCSC Ensembl
Innerchr15:49545009..49557933hg19UCSC Ensembl
Innerchr15:47332301..47345225hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3812925
hg1912925
hg1812925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569365
Supporting Variants
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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