A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133968



Internal ID19272901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7207472..7207530hg38UCSC Ensembl
Outerchr10:7249434..7249492hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985419, nssv3990394
SamplesKWS2, KWS1
Known GenesSFMBT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133968
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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