A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765729



Internal ID19309340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74979558..75065788hg38UCSC Ensembl
chr7:74393699..74481600hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3886231
hg1987902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075972
Supporting Variants
SamplesKWP1
Known GenesWBSCR16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765729
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