A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954725



Internal ID17303598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:168538937..168539260hg38UCSC Ensembl
Outerchr2:169395447..169395770hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003803
SamplesBILGI_BIOE
Known GenesCERS6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954725
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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