A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076015



Internal ID18978777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150977611..150978412hg38UCSC Ensembl
chr7:150674699..150675500hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769790
SamplesKWP1
Known GenesKCNH2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076015
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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