A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133406



Internal ID18909717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:45635434..45679134hg38UCSC Ensembl
Outerchr17:43712800..43756500hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3843701
hg1943701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967842
SamplesKWS2
Known GenesCRHR1, CRHR1-IT1, MGC57346
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133406
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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