A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109925



Internal ID18919076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152278676..152278738hg38UCSC Ensembl
Outerchr7:151975761..151975823hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3701n106
Supporting Variantsnssv3958363
SamplesKWS1
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109925
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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