A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998008



Internal ID17290960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:70528645..70542044hg38UCSC Ensembl
Outerchr10:72288401..72301800hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950976
Supporting Variants
SamplesBILGI_BIOE
Known GenesPALD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998008
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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