A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987740



Internal ID19219906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:88183330..88183406hg38UCSC Ensembl
Outerchr6:88893049..88893125hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132946
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987740
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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