A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984710



Internal ID19224840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:45620534..45621434hg38UCSC Ensembl
Outerchr17:43697900..43698800hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126461
Supporting Variants
SamplesKWS1
Known GenesCRHR1, MGC57346
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984710
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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