A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074451



Internal ID19326547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169765830..169765998hg38UCSC Ensembl
chr6:170165926..170166094hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763647
SamplesKWP1
Known GenesERMARD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074451
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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