A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124097



Internal ID19274023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:88091426..88092700hg38UCSC Ensembl
Outerchr6:88801144..88802418hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3346n106
Supporting Variantsnssv3970049, nssv3975813
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124097
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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