A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7957



Internal ID15535907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:55735732..55750007hg38UCSC Ensembl
Outerchr4:56601898..56616173hg19UCSC Ensembl
Outerchr4:56296655..56310930hg18UCSC Ensembl
Outerchr4:56442826..56457101hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386222
hg196222
hg186222
hg176222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4346
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv7957
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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