A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6411



Internal ID15190767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97271476..97310933hg38UCSC Ensembl
Outerchr10:99031233..99070690hg19UCSC Ensembl
Outerchr10:99021223..99060680hg18UCSC Ensembl
Outerchr10:99021223..99060680hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3839458
hg1939458
hg1839458
hg1739458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7507
Supporting Variants
SamplesNA12156
Known GenesARHGAP19, ARHGAP19-SLIT1
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)nssv6411
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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