A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110177



Internal ID18938424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77471042..77472542hg38UCSC Ensembl
Outerchr10:79230800..79232300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv482n106
Supporting Variantsnssv3959444
SamplesKWS1
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110177
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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