A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140862



Internal ID18932797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152408943..152408996hg38UCSC Ensembl
Outerchr7:152106028..152106081hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3705n106
Supporting Variantsnssv3992364
SamplesKWS2
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140862
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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