A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133660



Internal ID18914444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74658074..74658874hg38UCSC Ensembl
Outerchr7:74072400..74073200hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3592n106
Supporting Variantsnssv3969228
SamplesKWS2
Known GenesGTF2I
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133660
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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