A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127839



Internal ID19280416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:142840301..142840399hg38UCSC Ensembl
Outerchr6:143161438..143161536hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3407n106
Supporting Variantsnssv3956436
SamplesKWS1
Known GenesHIVEP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127839
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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