A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136564



Internal ID19275915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63543939..63543995hg38UCSC Ensembl
Outerchr20:62175292..62175348hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972950
SamplesKWS2
Known GenesSRMS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136564
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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