A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958654



Internal ID19224139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97867021..97867353hg38UCSC Ensembl
Outerchr7:97496333..97496665hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135682
Supporting Variants
SamplesKWS1
Known GenesASNS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958654
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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