A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002706



Internal ID19186859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138718221..138718347hg38UCSC Ensembl
Outerchr7:138402966..138403092hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149198
Supporting Variants
SamplesKWB1
Known GenesATP6V0A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002706
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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