A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952804



Internal ID16954991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150964125..150976324hg38UCSC Ensembl
Outerchr1:150936601..150948800hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997319
SamplesBILGI_BIOE
Known GenesCERS2, SETDB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952804
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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