A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140860



Internal ID18914892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152404164..152404215hg38UCSC Ensembl
Outerchr7:152101249..152101300hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n106
Supporting Variantsnssv3992362
SamplesKWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140860
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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