A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770733



Internal ID19309978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74964071..74965603hg38UCSC Ensembl
chr7:74378799..74379700hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381533
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075033
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770733
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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