A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109736



Internal ID18909989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:150205236..150205320hg38UCSC Ensembl
Outerchr5:149584799..149584883hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3193n106
Supporting Variantsnssv3958072
SamplesKWS1
Known GenesSLC6A7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109736
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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