A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771481



Internal ID19304632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1307719..1308120hg38UCSC Ensembl
chr1:1243099..1243500hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074967
Supporting Variants
SamplesKWP1
Known GenesACAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771481
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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