A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122069



Internal ID19252009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35033835..35034167hg38UCSC Ensembl
Outerchr20:33621638..33621970hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n106
Supporting Variantsnssv3969505
SamplesKWS1
Known GenesTRPC4AP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122069
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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