A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156268



Internal ID22084744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16542868..16679483hg38UCSC Ensembl
Outerchr1:16525019..16685015hg38UCSC Ensembl
Innerchr1:16869363..17005978hg19UCSC Ensembl
Outerchr1:16851514..17011510hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38159997
hg19159997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n97
Supporting Variantsnssv4019171
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156268
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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