A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119071



Internal ID18908464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:12010967..12012767hg38UCSC Ensembl
Outerchr6:12011200..12013000hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981871
SamplesKWS1
Known GenesHIVEP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119071
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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