A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133626



Internal ID18905338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:7108567..7109467hg38UCSC Ensembl
Outerchr6:7108800..7109700hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969566, nssv3985014
SamplesKWS2, KWS1
Known GenesRREB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133626
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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