A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122537



Internal ID19251538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71857387..71857438hg38UCSC Ensembl
Outerchr10:73617144..73617195hg19UCSC 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 Variantsnssv3970746
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122537
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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