A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956640



Internal ID17305513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:41635534..41635614hg38UCSC Ensembl
Outerchr1:42101205..42101285hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000480
SamplesBILGI_BIOE
Known GenesHIVEP3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956640
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