A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956186



Internal ID18875670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19800955..19801006hg38UCSC Ensembl
Outerchr19:19911764..19911815hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127664
Supporting Variants
SamplesKWS1
Known GenesZNF506
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956186
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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