A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005560



Internal ID17298512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63789149..63789271hg38UCSC Ensembl
Outerchr15:64081348..64081470hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958028
Supporting Variants
SamplesBILGI_BIOE
Known GenesHERC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005560
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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