A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077905



Internal ID18974298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67709978..67710216hg38UCSC Ensembl
chr1:68175661..68175899hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770025
SamplesKWP1
Known GenesGNG12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077905
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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