A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956748



Internal ID18859206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:85874758..85874814hg38UCSC Ensembl
Outerchr4:86795911..86795967hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136884
Supporting Variants
SamplesKWS1
Known GenesARHGAP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956748
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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