A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv910



Internal ID15206245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:54605786..54663322hg38UCSC Ensembl
Outerchr1:55071459..55128995hg19UCSC Ensembl
Outerchr1:54844047..54901583hg18UCSC Ensembl
Outerchr1:54783480..54841016hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3857537
hg1957537
hg1857537
hg1757537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6611, nssv2142
SamplesNA12156, NA18555
Known GenesACOT11, FAM151A, MROH7, MROH7-TTC4
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)nsv910
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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