A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980285



Internal ID18875713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35077127..35081853hg38UCSC Ensembl
Outerchr22:35473120..35477846hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118076
Supporting Variants
SamplesKWS1
Known GenesISX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980285
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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