A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526707



Internal ID15107314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39354904..39359315hg38UCSC Ensembl
Innerchr19:39845544..39849955hg19UCSC Ensembl
Innerchr19:44537384..44541795hg18UCSC Ensembl
Innerchr19:44537384..44541795hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg384412
hg194412
hg184412
hg174412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv202n21
Supporting Variantsnssv703046
Samples
Known GenesSAMD4B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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