A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137879



Internal ID18927958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13873734..13873798hg38UCSC Ensembl
Outerchr10:13915734..13915798hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985427, nssv3970305
SamplesKWS1, KWS2
Known GenesFRMD4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137879
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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