A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954934



Internal ID19205764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57820705..57820768hg38UCSC Ensembl
Outerchr17:55898066..55898129hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109089
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954934
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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