A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112903



Internal ID19262777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99349424..99349924hg38UCSC Ensembl
Outerchr6:99797300..99797800hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967404
SamplesKWS2
Known GenesFAXC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112903
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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