A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963580



Internal ID19230328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:24809155..24809497hg38UCSC Ensembl
Outerchr10:25098084..25098426hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111445
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963580
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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