A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985125



Internal ID19215841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:21767188..21804588hg38UCSC Ensembl
Outerchr8:21624700..21662100hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3837401
hg1937401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126849
Supporting Variants
SamplesKWS1
Known GenesGFRA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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