A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709150



Internal ID15656420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6161915..6262876hg38UCSC Ensembl
Innerchr1:6221975..6322936hg19UCSC Ensembl
Innerchr1:6144562..6245523hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38100962
hg19100962
hg18100962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545236
Supporting Variants
Samples
Known GenesCHD5, GPR153, HES3, ICMT, LINC00337, RNF207, RPL22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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