A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951002



Internal ID16953189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:100723244..100761943hg38UCSC Ensembl
Outerchr10:102483001..102521700hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3838700
hg1938700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998034
SamplesBILGI_BIOE
Known GenesPAX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951002
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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