A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133600



Internal ID19278549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:61425644..61437518hg38UCSC Ensembl
Outerchr20:60000700..60012574hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811875
hg1911875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2278n106
Supporting Variantsnssv3969164
SamplesKWS1
Known GenesCDH4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133600
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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