A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970290



Internal ID18888751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1213943..1214003hg38UCSC Ensembl
Outerchr10:1259883..1259943hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133960
Supporting Variants
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970290
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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