A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970365



Internal ID18879964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71839363..71839429hg38UCSC Ensembl
Outerchr10:73599120..73599186hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134025
Supporting Variants
SamplesKWS2
Known GenesPSAP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970365
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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