A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076881



Internal ID19321759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27113780..27114081hg38UCSC Ensembl
chr7:27153399..27153700hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766259
SamplesKWP1
Known GenesHOXA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076881
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