A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569355



Internal ID16010078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49252812..49254227hg38UCSC Ensembl
Innerchr15:49545009..49546424hg19UCSC Ensembl
Innerchr15:47332301..47333716hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381416
hg191416
hg181416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4518n54
Supporting Variantsnssv842547, nssv842548, nssv842545, nssv842543, nssv842542, nssv842541, nssv842546, nssv842544
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569355
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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