A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005478



Internal ID17298430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25686261..25687228hg38UCSC Ensembl
Outerchr15:25931408..25932375hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958808
Supporting Variants
SamplesBILGI_BIOE
Known GenesATP10A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005478
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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