A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998088



Internal ID17291040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132551897..132555096hg38UCSC Ensembl
Outerchr10:134365401..134368600hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952698
Supporting Variants
SamplesBILGI_BIOE
Known GenesINPP5A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998088
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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