A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126740



Internal ID18905639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:1313265..1313765hg38UCSC Ensembl
Outerchr6:1313500..1314000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985008
SamplesKWS1
Known GenesFOXQ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126740
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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