A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952637



Internal ID16954824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:201647873..201655872hg38UCSC Ensembl
Outerchr1:201617001..201625000hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999173
SamplesBILGI_BIOE
Known GenesNAV1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952637
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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