A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118996



Internal ID18932986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7192373..7192973hg38UCSC Ensembl
Outerchr4:7194100..7194700hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2724n106
Supporting Variantsnssv3981789
SamplesKWS1
Known GenesSORCS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118996
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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