A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962173



Internal ID19210856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74726836..74726899hg38UCSC Ensembl
Outerchr7:74141170..74141237hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3864
hg1968
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120547
Supporting Variants
SamplesKWS1
Known GenesGTF2I
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962173
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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