A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975642



Internal ID18862209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1409940..1410020hg38UCSC Ensembl
Outerchr10:1452135..1452215hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124342
Supporting Variants
SamplesKWS1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975642
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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