A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6101



Internal ID15537762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160614634..160663627hg38UCSC Ensembl
Outerchr6:161035666..161084659hg19UCSC Ensembl
Outerchr6:160955656..161004649hg18UCSC Ensembl
Outerchr6:161006077..161055070hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3848994
hg1948994
hg1848994
hg1748994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5567
Supporting Variants
SamplesNA12156
Known GenesLPA
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)nssv6101
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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