A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074411



Internal ID19319509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73711548..73711934hg38UCSC Ensembl
chr6:74421271..74421657hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772346
SamplesKWP1
Known GenesCD109
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074411
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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