A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4624



Internal ID15543336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93034531..93042280hg38UCSC Ensembl
Outerchr10:94794288..94802037hg19UCSC Ensembl
Outerchr10:94784268..94792017hg18UCSC Ensembl
Outerchr10:94784268..94792017hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg387750
hg197750
hg187750
hg177750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7493
Supporting Variants
SamplesNA19129
Known GenesEXOC6
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)nssv4624
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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