A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959641



Internal ID19214178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:116816537..116820137hg38UCSC Ensembl
Outerchr6:117137700..117141300hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119207
Supporting Variants
SamplesKWS1
Known GenesGPRC6A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959641
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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