A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992805



Internal ID18887618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:16752686..16845386hg38UCSC Ensembl
Outerchr17:16656000..16748700hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3892701
hg1992701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141300
Supporting Variants
SamplesKWS2
Known GenesCCDC144A, FAM106CP, KRT16P2, USP32P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992805
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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