A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958396



Internal ID17307269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:4907591..4910538hg38UCSC Ensembl
Outerchr1:4967651..4970598hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382948
hg192948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003727
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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