A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765914



Internal ID19304805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79700969..79701694hg38UCSC Ensembl
chr17:77674799..77675500hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38726
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072758
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765914
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