A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074189



Internal ID19325174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74936559..74942626hg38UCSC Ensembl
chr4:75861769..75867836hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772471
SamplesKWP1
Known GenesPARM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074189
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