A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122538



Internal ID18910623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71996402..71996453hg38UCSC Ensembl
Outerchr10:73756160..73756211hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995312, nssv3970747
SamplesKWS1, KWS2
Known GenesCHST3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122538
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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