A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573



Internal ID15550396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160768429..160797287hg38UCSC Ensembl
Outerchr6:161189461..161218319hg19UCSC Ensembl
Outerchr6:161109451..161138309hg18UCSC Ensembl
Outerchr6:161159872..161188730hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg387855
hg197855
hg187855
hg177855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6103, nssv598, nssv2625
SamplesNA12156, NA18555, NA19240
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)nsv5573
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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