A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136236



Internal ID19286002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:45782934..45815334hg38UCSC Ensembl
Outerchr17:43860300..43892700hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3832401
hg1932401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1474n106
Supporting Variantsnssv3989848
SamplesKWS2
Known GenesCRHR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136236
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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