A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977107



Internal ID19227002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35475572..35479672hg38UCSC Ensembl
Outerchr10:35764500..35768600hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139519
Supporting Variants
SamplesKWS2
Known GenesCCNY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977107
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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