A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013865



Internal ID18756397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16627264..16679269hg38UCSC Ensembl
Innerchr1:16953759..17005764hg19UCSC Ensembl
Innerchr1:16826346..16878351hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3852006
hg1952006
hg1852006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv71n100
Supporting Variantsnssv3477072
Samples
Known GenesCROCCP2, LOC729574, MST1P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013865
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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