A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964109



Internal ID19234856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:7502711..7502974hg38UCSC Ensembl
Outerchr7:7542342..7542605hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120901
Supporting Variants
SamplesKWS2
Known GenesCOL28A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964109
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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