A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950958



Internal ID16953145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46108622..46110521hg38UCSC Ensembl
Outerchr10:51485301..51487200hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997990
SamplesBILGI_BIOE
Known GenesAGAP7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950958
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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