A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951400



Internal ID16953587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1889362..1943761hg38UCSC Ensembl
Outerchr1:1820801..1875200hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3854400
hg1954400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997204
SamplesBILGI_BIOE
Known GenesCALML6, GNB1, TMEM52
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951400
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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