A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121369



Internal ID19250573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:36313063..36313148hg38UCSC Ensembl
Outerchr7:36352672..36352757hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3526n106
Supporting Variantsnssv3991499, nssv3989244
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121369
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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