A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109803



Internal ID19286012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:87941590..87941662hg38UCSC Ensembl
Outerchr6:88651308..88651380hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958169
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109803
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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