A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973121



Internal ID18890488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:57761818..57761874hg38UCSC Ensembl
Outerchr3:57747545..57747601hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136726
Supporting Variants
SamplesKWS2
Known GenesSLMAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973121
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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