A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986789



Internal ID19213736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155263091..155263234hg38UCSC Ensembl
Outerchr7:155054801..155054944hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132109
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986789
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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