A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973510



Internal ID19217649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:78771162..78771252hg38UCSC Ensembl
Outerchr8:79683397..79683487hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123737
Supporting Variants
SamplesKWS1
Known GenesIL7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973510
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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