A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2737657



Internal ID17878841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62503501..62519679hg38UCSC Ensembl
Innerchr9:46814802..46830980hg19UCSC Ensembl
Innerchr9:46654798..46670976hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816179
hg1916179
hg1816179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv973657
Supporting Variants
SamplesHGDP01307
Known GenesLOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2737657
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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