A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955777



Internal ID16957964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:94773931..94774260hg38UCSC Ensembl
Outerchr5:94109636..94109965hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002068
SamplesBILGI_BIOE
Known GenesMCTP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955777
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer