A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117961



Internal ID18928077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:7756555..7756647hg38UCSC Ensembl
Outerchr4:7758282..7758374hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980163
SamplesKWS1
Known GenesAFAP1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117961
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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