A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766005



Internal ID19314737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6260939..6261240hg38UCSC Ensembl
chr1:6320999..6321300hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076029
Supporting Variants
SamplesKWP1
Known GenesGPR153
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766005
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