A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126250



Internal ID18938717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:44292752..44293252hg38UCSC Ensembl
Outerchr10:44788200..44788700hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984483
SamplesKWS1
Known GenesLOC100130539
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126250
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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