A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952504



Internal ID17301378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:128843856..128849655hg38UCSC Ensembl
Outerchr12:129328401..129334200hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997378
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952504
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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