A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954553



Internal ID19220104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:33175474..33175529hg38UCSC Ensembl
Outerchr17:31502492..31502547hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116213
Supporting Variants
SamplesKWS1
Known GenesASIC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954553
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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