A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766437



Internal ID18961400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74453769..74454370hg38UCSC Ensembl
chr7:73868099..73868700hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076927
Supporting Variants
SamplesKWP1
Known GenesGTF2IRD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766437
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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