A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076879



Internal ID18977864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26183424..26183575hg38UCSC Ensembl
chr7:26223044..26223195hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767073
SamplesKWP1
Known GenesNFE2L3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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