A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958302



Internal ID19213096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:75664086..75664165hg38UCSC Ensembl
Outerchr7:75293404..75293483hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137257
Supporting Variants
SamplesKWS1
Known GenesHIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958302
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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