A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767189



Internal ID19306743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100951071..100951572hg38UCSC Ensembl
chr8:101963299..101963800hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077061
Supporting Variants
SamplesKWP1
Known GenesYWHAZ
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767189
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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