A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957895



Internal ID19219551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:128489927..128510773hg38UCSC Ensembl
Outerchr7:128129981..128150827hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3820847
hg1920847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117759
Supporting Variants
SamplesKWS1
Known GenesMETTL2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957895
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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