A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2031197



Internal ID17772539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75479999..75484614hg38UCSC Ensembl
Innerchr15:75772340..75776955hg19UCSC Ensembl
Innerchr15:73559393..73564010hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384616
hg194616
hg184618
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv977738
Supporting Variants
SamplesHGDP00542
Known GenesPTPN9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2031197
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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