A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010082



Internal ID18752613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16470226..16935740hg38UCSC Ensembl
Innerchr1:16796721..17262235hg19UCSC Ensembl
Innerchr1:16669308..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38465515
hg19465515
hg18465515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39n100
Supporting Variantsnssv3469676
Samples
Known GenesCROCC, CROCCP2, CROCCP3, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010082
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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