A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950997



Internal ID16953184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:95762744..95809443hg38UCSC Ensembl
Outerchr10:97522501..97569200hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3846700
hg1946700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998029
SamplesBILGI_BIOE
Known GenesENTPD1, ENTPD1-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950997
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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