A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003602



Internal ID18746133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16627264..16660344hg38UCSC Ensembl
Innerchr1:16953759..16986839hg19UCSC Ensembl
Innerchr1:16826346..16859426hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3833081
hg1933081
hg1833081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3470239, nssv3464884
Samples
Known GenesCROCCP2, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003602
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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