A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074545



Internal ID18976222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107679954..107680355hg38UCSC Ensembl
chr7:107320399..107320800hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771156
SamplesKWP1
Known GenesSLC26A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074545
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