A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140599



Internal ID18940078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:4116503..4116566hg38UCSC Ensembl
Outerchr6:4116737..4116800hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992101
SamplesKWS2
Known GenesC6orf201, ECI2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140599
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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