A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958653



Internal ID16960840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:32810686..32810984hg38UCSC Ensembl
Outerchr12:32963620..32963918hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004087
SamplesBILGI_BIOE
Known GenesPKP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958653
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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