A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137113



Internal ID19285611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:73711530..73711836hg38UCSC Ensembl
Outerchr6:74421253..74421559hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975125, nssv3986626
SamplesKWS2, KWS1
Known GenesCD109
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137113
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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