A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981852



Internal ID18864839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177446699..177447599hg38UCSC Ensembl
Outerchr5:176873700..176874600hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119054
Supporting Variants
SamplesKWS1
Known GenesPRR7, PRR7-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981852
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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