A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004895



Internal ID18747426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909177..16931137hg38UCSC Ensembl
Innerchr1:17235672..17257632hg19UCSC Ensembl
Innerchr1:17108259..17130219hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821961
hg1921961
hg1821961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3471492
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004895
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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