A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9907



Internal ID15539989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:217997109..218032128hg38UCSC Ensembl
Outerchr1:218170451..218205470hg19UCSC Ensembl
Outerchr1:216237074..216272093hg18UCSC Ensembl
Outerchr1:214558846..214593865hg17UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3835020
hg1935020
hg1835020
hg1735020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4587
Supporting Variants
SamplesNA18507
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)nssv9907
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer