A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145971



Internal ID19197587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:22431270..22431363hg38UCSC Ensembl
Outerchr4:22432893..22432986hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997334
SamplesKWB1
Known GenesGPR125
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1145971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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