A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969227



Internal ID18884326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:73600270..73600970hg38UCSC Ensembl
Outerchr7:73014600..73015300hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133659
Supporting Variants
SamplesKWS2
Known GenesMLXIPL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969227
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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