A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115028



Internal ID18928459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152278676..152278747hg38UCSC Ensembl
Outerchr7:151975761..151975832hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3701n106
Supporting Variantsnssv3975331
SamplesKWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115028
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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