A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110534



Internal ID19270745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:61425244..61438644hg38UCSC Ensembl
Outerchr20:60000300..60013700hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2278n106
Supporting Variantsnssv3960187
SamplesKWS1
Known GenesCDH4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110534
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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