A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999076



Internal ID16945342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35236600..35241999hg38UCSC Ensembl
Outerchr15:35528801..35534200hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952609
Supporting Variants
SamplesBILGI_BIOE
Known GenesANP32AP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999076
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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