A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962884



Internal ID18866701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71701815..71701897hg38UCSC Ensembl
Outerchr7:71166800..71166882hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129437
Supporting Variants
SamplesKWS1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962884
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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